Features Table
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PhenoDB ID | PhenoDB Feature Path | HPO ID | ICHPT ID | Elements of Morphology ID |
---|---|---|---|---|
phenodb:0001 | GROWTH & BUILD: | |||
phenodb:0002 | GROWTH & BUILD: Current growth and build | |||
phenodb:0003 | GROWTH & BUILD: Current growth and build > Height | HP:0000002 | ||
phenodb:0004 | GROWTH & BUILD: Current growth and build > Height > Short | HP:0004322 | T2839 | |
phenodb:0005 | GROWTH & BUILD: Current growth and build > Height > Short > Proportionate | HP:0003508 | T2840 | |
phenodb:0006 | GROWTH & BUILD: Current growth and build > Height > Short > Disproportionate, short limbs | HP:0008873 | T2841 | |
phenodb:0007 | GROWTH & BUILD: Current growth and build > Height > Short > Disproportionate, short trunk | HP:0008922 | ||
phenodb:0008 | GROWTH & BUILD: Current growth and build > Height > Short > Other feature | |||
phenodb:0009 | GROWTH & BUILD: Current growth and build > Height > Tall | HP:0000098 | T2834 | |
phenodb:0010 | GROWTH & BUILD: Current growth and build > Height > Tall > Proportionate | HP:0011407 | T2835 | |
phenodb:2925 | GROWTH & BUILD: Current growth and build > Height > Tall > Disproportionate | HP:0001519 | ||
phenodb:0011 | GROWTH & BUILD: Current growth and build > Height > Tall > Disproportionate, long limbs | |||
phenodb:0012 | GROWTH & BUILD: Current growth and build > Height > Tall > Disproportionate, long trunk | |||
phenodb:0013 | GROWTH & BUILD: Current growth and build > Height > Tall > Other feature | |||
phenodb:0014 | GROWTH & BUILD: Current growth and build > Weight | HP:0004323 | ||
phenodb:0015 | GROWTH & BUILD: Current growth and build > Weight > Underweight | HP:0004325 | ||
phenodb:0016 | GROWTH & BUILD: Current growth and build > Weight > Underweight > Isolated (height average or tall) | |||
phenodb:0017 | GROWTH & BUILD: Current growth and build > Weight > Underweight > With short stature | |||
phenodb:0018 | GROWTH & BUILD: Current growth and build > Weight > Underweight > Other feature | |||
phenodb:0019 | GROWTH & BUILD: Current growth and build > Weight > Overweight | HP:0004324 | ||
phenodb:0020 | GROWTH & BUILD: Current growth and build > Weight > Overweight > Isolated (height average or short) | |||
phenodb:0021 | GROWTH & BUILD: Current growth and build > Weight > Overweight > With tall stature | |||
phenodb:0022 | GROWTH & BUILD: Current growth and build > Weight > Overweight > Other feature | |||
phenodb:0023 | GROWTH & BUILD: Birth growth parameters | |||
phenodb:0024 | GROWTH & BUILD: Birth growth parameters > Length | |||
phenodb:0025 | GROWTH & BUILD: Birth growth parameters > Length > Small for gestational age (<10%) | HP:0001518 | T2843 | |
phenodb:0026 | GROWTH & BUILD: Birth growth parameters > Length > Large for gestational age (>90%) | HP:0001520 | ||
phenodb:0027 | GROWTH & BUILD: Birth growth parameters > Length > Other feature | |||
phenodb:0028 | GROWTH & BUILD: Birth growth parameters > Weight | |||
phenodb:0029 | GROWTH & BUILD: Birth growth parameters > Weight > Small for gestational age (<10%) | HP:0001518 | ||
phenodb:0030 | GROWTH & BUILD: Birth growth parameters > Weight > Large for gestational age (>90%) | HP:0001520 | ||
phenodb:0031 | GROWTH & BUILD: Birth growth parameters > Weight > Other feature | |||
phenodb:0032 | GROWTH & BUILD: Birth growth parameters > Head circumference | |||
phenodb:0033 | GROWTH & BUILD: Birth growth parameters > Head circumference > Small for gestational age (<10%) | HP:0011451 | ||
phenodb:0034 | GROWTH & BUILD: Birth growth parameters > Head circumference > Large for gestational age (>90%) | HP:0004488 | ||
phenodb:0035 | GROWTH & BUILD: Birth growth parameters > Head circumference > Other feature | |||
phenodb:0036 | GROWTH & BUILD: Other growth characteristics | |||
phenodb:0037 | GROWTH & BUILD: Other growth characteristics > Abnormal fat distribution | HP:0007552 | T2827 | |
phenodb:2926 | GROWTH & BUILD: Other growth characteristics > Body asymmetry | |||
phenodb:0038 | GROWTH & BUILD: Other growth characteristics > Cachexia | HP:0004326 | T2823 | |
phenodb:0039 | GROWTH & BUILD: Other growth characteristics > Dolichostenomelia | HP:0001519 | T2931 | |
phenodb:0040 | GROWTH & BUILD: Other growth characteristics > Failure to thrive | HP:0001508 | T2848 | |
phenodb:2927 | GROWTH & BUILD: Other growth characteristics > Hemiatrophy | HP:0100556 | T2844 | |
phenodb:0041 | GROWTH & BUILD: Other growth characteristics > Hemihypertrophy - generalized (one side of body) | HP:0001528 | ||
phenodb:0042 | GROWTH & BUILD: Other growth characteristics > Hemihypertrophy - isolated (specify body part below) | HP:0001528 | ||
phenodb:0043 | GROWTH & BUILD: Other growth characteristics > Hemihypertrophy - isolated (specify body part below) > Specify body part | |||
phenodb:0044 | GROWTH & BUILD: Other growth characteristics > Intrauterine growth retardation | HP:0001511 | ||
phenodb:0045 | GROWTH & BUILD: Other growth characteristics > Muscular | |||
phenodb:3631 | GROWTH & BUILD: Other growth characteristics > Obesity | HP:0001513 | T2825 | |
phenodb:0046 | GROWTH & BUILD: Other growth characteristics > Overgrowth | HP:0001548 | ||
phenodb:2928 | GROWTH & BUILD: Other growth characteristics > Premature aging | |||
phenodb:0047 | GROWTH & BUILD: Other growth characteristics > Thin | HP:0001533 | ||
phenodb:0048 | GROWTH & BUILD: Other growth characteristics > Truncal obesity | HP:0001956 | T2826 | |
phenodb:2865 | GROWTH & BUILD: Other growth characteristics > Other feature | |||
phenodb:0049 | HEAD AND NECK: | |||
phenodb:0050 | HEAD AND NECK: Head | HP:0000234 | ||
phenodb:0051 | HEAD AND NECK: Head > Size | |||
phenodb:0052 | HEAD AND NECK: Head > Size > Microcephaly | HP:0000252 | T0031 | 8ae2118220c1308f |
phenodb:0053 | HEAD AND NECK: Head > Size > Microcephaly > Primary (present since birth) | HP:0011451 | T0032 | |
phenodb:0054 | HEAD AND NECK: Head > Size > Microcephaly > Acquired (developed over time) | HP:0005484 | ||
phenodb:0055 | HEAD AND NECK: Head > Size > Microcephaly > Other feature | |||
phenodb:0056 | HEAD AND NECK: Head > Size > Macrocephaly | HP:0000256 | T0028 | 1d53660e657259f0 |
phenodb:0057 | HEAD AND NECK: Head > Size > Macrocephaly > Primary (present since birth) | HP:0004488 | T0029 | |
phenodb:0058 | HEAD AND NECK: Head > Size > Macrocephaly > Acquired (developed over time) | HP:0005490 | ||
phenodb:0059 | HEAD AND NECK: Head > Size > Macrocephaly > Other feature | |||
phenodb:0060 | HEAD AND NECK: Head > Shape | |||
phenodb:0061 | HEAD AND NECK: Head > Shape > Brachycephaly | HP:0000248 | T0050 | babe3e4648eac88a |
phenodb:0062 | HEAD AND NECK: Head > Shape > Dolichocephaly | HP:0000268 | e09c1185a1ef3e38 | |
phenodb:0063 | HEAD AND NECK: Head > Shape > Kleebattschadel / Clover-leaf skull | HP:0002676 | T0046 | 784956e8f2b55a24 |
phenodb:0064 | HEAD AND NECK: Head > Shape > Occipital abnormality | HP:0011217 | ||
phenodb:0065 | HEAD AND NECK: Head > Shape > Occipital abnormality > Flat | HP:0005469 | T0051 | 5e0e98c91707b90a |
phenodb:0066 | HEAD AND NECK: Head > Shape > Occipital abnormality > Prominent | HP:0000269 | T0052 | be559f6b4bd52c20 |
phenodb:0067 | HEAD AND NECK: Head > Shape > Occipital abnormality > Other feature | |||
phenodb:0068 | HEAD AND NECK: Head > Shape > Plagiocephaly | HP:0001357 | T0049 | 325a0c57c4817952 |
phenodb:0069 | HEAD AND NECK: Head > Shape > Scaphocephaly | HP:0000268 | T0047 | e09c1185a1ef3e38 |
phenodb:0070 | HEAD AND NECK: Head > Shape > Trigonocephaly | HP:0000243 | T0048 | 46937dc619ed9c29 |
phenodb:0071 | HEAD AND NECK: Head > Shape > Turricephaly | HP:0000262 | T0035 | b1c6362251bad427 |
phenodb:2866 | HEAD AND NECK: Head > Shape > Other feature | |||
phenodb:0072 | HEAD AND NECK: Head > Bone | HP:0000929 | T0001 | |
phenodb:0073 | HEAD AND NECK: Head > Bone > Fontanelle(s) | HP:0011328 | T0053 | |
phenodb:0074 | HEAD AND NECK: Head > Bone > Fontanelle(s) > Delayed closure | HP:0000270 | T0055 | |
phenodb:0075 | HEAD AND NECK: Head > Bone > Fontanelle(s) > Early closure | HP:0005458 | T0054 | |
phenodb:0076 | HEAD AND NECK: Head > Bone > Fontanelle(s) > Extra | HP:0012800 | ||
phenodb:0077 | HEAD AND NECK: Head > Bone > Fontanelle(s) > Large | HP:0000239 | T0057 | |
phenodb:0078 | HEAD AND NECK: Head > Bone > Fontanelle(s) > Small | HP:0005486 | T0058 | |
phenodb:0079 | HEAD AND NECK: Head > Bone > Fontanelle(s) > Other feature | |||
phenodb:0080 | HEAD AND NECK: Head > Bone > Foramen magnum, large | HP:0002700 | T0021 | |
phenodb:0081 | HEAD AND NECK: Head > Bone > Foramen magnum, small | HP:0002677 | T0020 | |
phenodb:0082 | HEAD AND NECK: Head > Bone > J-shaped sella turcica | HP:0002680 | T0015 | |
phenodb:2929 | HEAD AND NECK: Head > Bone > Anomaly of the sella turcica | HP:0002679 | T0013 | |
phenodb:2930 | HEAD AND NECK: Head > Bone > Large sella turcica | HP:0002690 | T0014 | |
phenodb:2931 | HEAD AND NECK: Head > Bone > Small sella turcica | HP:0010538 | T0016 | |
phenodb:0083 | HEAD AND NECK: Head > Bone > Sutures | HP:0011329 | T0010 | |
phenodb:0084 | HEAD AND NECK: Head > Bone > Sutures > Craniosynostosis | HP:0001363 | T0033 | |
phenodb:0085 | HEAD AND NECK: Head > Bone > Sutures > Craniosynostosis > Coronal | HP:0004440 | T0041 | |
phenodb:0086 | HEAD AND NECK: Head > Bone > Sutures > Craniosynostosis > Coronal > Unilateral | HP:0011315 | T0042 | |
phenodb:0087 | HEAD AND NECK: Head > Bone > Sutures > Craniosynostosis > Coronal > Bilateral | HP:0011318 | T0043 | |
phenodb:0088 | HEAD AND NECK: Head > Bone > Sutures > Craniosynostosis > Lambdoidal | HP:0004443 | T0038 | |
phenodb:0089 | HEAD AND NECK: Head > Bone > Sutures > Craniosynostosis > Lambdoidal > Unilateral | HP:0011320 | ||
phenodb:0090 | HEAD AND NECK: Head > Bone > Sutures > Craniosynostosis > Lambdoidal > Bilateral | HP:0011319 | T0040 | |
phenodb:0091 | HEAD AND NECK: Head > Bone > Sutures > Craniosynostosis > Metopic | HP:0011330 | T0044 | |
phenodb:0092 | HEAD AND NECK: Head > Bone > Sutures > Craniosynostosis > Sagittal | HP:0004442 | T0045 | |
phenodb:0093 | HEAD AND NECK: Head > Bone > Sutures > Metopic depressed | HP:0011223 | d704aa52d376aaa5 | |
phenodb:0094 | HEAD AND NECK: Head > Bone > Sutures > Metopic prominent | HP:0005487 | T0060 | 6ab37326cc1eed1d |
phenodb:0095 | HEAD AND NECK: Head > Bone > Sutures > Ridged, general | HP:0010823 | T0012 | |
phenodb:0096 | HEAD AND NECK: Head > Bone > Sutures > Wide, general | HP:0010537 | T0011 | |
phenodb:0097 | HEAD AND NECK: Head > Bone > Orbits, shallow | HP:0000586 | ||
phenodb:3632 | HEAD AND NECK: Head > Bone > Orbital cyst | HP:0001144 | T0027 | |
phenodb:0098 | HEAD AND NECK: Head > Bone > Ossification defect | HP:0005474 | T0008 | |
phenodb:0099 | HEAD AND NECK: Head > Bone > Over mineralized, sclerotic | HP:0004437 | T0003 | |
phenodb:0100 | HEAD AND NECK: Head > Bone > Paranasal sinus, absent or small | HP:0002689 | ||
phenodb:0101 | HEAD AND NECK: Head > Bone > Parietal foramina | HP:0002697 | T0066 | |
phenodb:0102 | HEAD AND NECK: Head > Bone > Platybasia | HP:0002691 | T0063 | |
phenodb:3633 | HEAD AND NECK: Head > Bone > Calvarial Hyperostosis | HP:0004490 | T0005 | |
phenodb:0103 | HEAD AND NECK: Head > Bone > Under mineralized, soft, compressible | HP:0004331 | T0006 | |
phenodb:0104 | HEAD AND NECK: Head > Bone > Wormian bones | HP:0002645 | T0064 | |
phenodb:2932 | HEAD AND NECK: Head > Bone > Basilar hyperostosis | HP:0002694 | T0004 | |
phenodb:3634 | HEAD AND NECK: Head > Bone > Anomaly of the temporal bone | HP:0009911 | T0018 | |
phenodb:3635 | HEAD AND NECK: Head > Bone > Anomaly of the mastoid process | HP:0000264 | T0019 | |
phenodb:2867 | HEAD AND NECK: Head > Bone > Other feature | |||
phenodb:0105 | HEAD AND NECK: Head > Scalp | HP:0001965 | ||
phenodb:0106 | HEAD AND NECK: Head > Scalp > Cutis aplasia | HP:0007385 | T0062 | |
phenodb:2933 | HEAD AND NECK: Head > Scalp > Cutis gyrata | HP:0010541 | T1366 | |
phenodb:2934 | HEAD AND NECK: Head > Scalp > Hypersensitivity | HP:0100809 | T1370 | |
phenodb:0108 | HEAD AND NECK: Head > Scalp > Other feature | |||
phenodb:0109 | HEAD AND NECK: Head > Hair | HP:0001595 | ||
phenodb:0110 | HEAD AND NECK: Head > Hair > Growth | HP:0011363 | ||
phenodb:0111 | HEAD AND NECK: Head > Hair > Growth > Alopecia | HP:0001596 | T1337 | |
phenodb:0112 | HEAD AND NECK: Head > Hair > Growth > Excessive | HP:0100874 | ||
phenodb:2935 | HEAD AND NECK: Head > Hair > Growth > Thick | HP:0100874 | T1354 | |
phenodb:0113 | HEAD AND NECK: Head > Hair > Growth > Slow / No growth | HP:0002217 | T1348 | |
phenodb:0114 | HEAD AND NECK: Head > Hair > Growth > Sparse | HP:0002209 | T1330 | 40d80f6dcc04b2c1 |
phenodb:0115 | HEAD AND NECK: Head > Hair > Growth > Other feature | |||
phenodb:0116 | HEAD AND NECK: Head > Hair > Pattern | HP:0010720 | T1362 | |
phenodb:2936 | HEAD AND NECK: Head > Hair > Pattern > Frontal balding | HP:0002292 | T1361 | |
phenodb:0117 | HEAD AND NECK: Head > Hair > Pattern > Frontal upsweep or cowlick | HP:0002236 | T0076 | d9938e4ead4ace7c |
phenodb:2937 | HEAD AND NECK: Head > Hair > Pattern > Abnormal hairline position | HP:0009553 | T1364 | |
phenodb:0118 | HEAD AND NECK: Head > Hair > Pattern > Abnormal hairline position > High anterior hairline | HP:0009890 | T1368 | f635aa5bd991cae4 |
phenodb:0119 | HEAD AND NECK: Head > Hair > Pattern > Abnormal hairline position > Low anterior hairline | HP:0000294 | T0077 | 371fa772c36e1ca9 |
phenodb:0120 | HEAD AND NECK: Head > Hair > Pattern > Low posterior hairline | HP:0002162 | T1367 | efe02d35c10721b6 |
phenodb:2938 | HEAD AND NECK: Head > Hair > Pattern > Whorl, abnormal position | HP:0010814 | T1365 | |
phenodb:0121 | HEAD AND NECK: Head > Hair > Pattern > Whorls, abnormal (more than 2 clockwise hair whorls) | HP:0010813 | T6009 | f3795f87c4abb99d |
phenodb:0122 | HEAD AND NECK: Head > Hair > Pattern > Widow's peak | HP:0000349 | T1369 | b1adb2541073344c |
phenodb:0123 | HEAD AND NECK: Head > Hair > Pattern > Other feature | |||
phenodb:0124 | HEAD AND NECK: Head > Hair > Texture | HP:0010719 | T1350 | |
phenodb:0125 | HEAD AND NECK: Head > Hair > Texture > Brittle | HP:0002299 | ||
phenodb:0126 | HEAD AND NECK: Head > Hair > Texture > Coarse | HP:0002208 | T1353 | |
phenodb:0127 | HEAD AND NECK: Head > Hair > Texture > Fine / Thin | HP:0002213 | T1352 | |
phenodb:0128 | HEAD AND NECK: Head > Hair > Texture > Kinky | HP:0002212 | T1356 | |
phenodb:2939 | HEAD AND NECK: Head > Hair > Texture > Pili torti | HP:0003777 | T1359 | |
phenodb:2940 | HEAD AND NECK: Head > Hair > Texture > Wooly | HP:0002224 | T1357 | |
phenodb:0129 | HEAD AND NECK: Head > Hair > Texture > Other feature | |||
phenodb:0130 | HEAD AND NECK: Head > Hair > Color | HP:0002286 | ||
phenodb:0131 | HEAD AND NECK: Head > Hair > Color > Blond | HP:0002286 | T1343 | |
phenodb:0132 | HEAD AND NECK: Head > Hair > Color > Premature grey | HP:0002216 | T1341 | |
phenodb:0133 | HEAD AND NECK: Head > Hair > Color > Red | HP:0002297 | ||
phenodb:0134 | HEAD AND NECK: Head > Hair > Color > White forelock | HP:0002211 | T1347 | |
phenodb:0135 | HEAD AND NECK: Head > Hair > Color > White patches | HP:0007544 | T1346 | |
phenodb:0136 | HEAD AND NECK: Head > Hair > Color > White generalized | HP:0011364 | T1344 | |
phenodb:0137 | HEAD AND NECK: Head > Hair > Color > Other feature | |||
phenodb:0138 | HEAD AND NECK: Face | HP:0000271 | ||
phenodb:0139 | HEAD AND NECK: Face > General abnormalities | HP:0000271 | ||
phenodb:0140 | HEAD AND NECK: Face > General abnormalities > Structure | HP:0000271 | T0078 | |
phenodb:0141 | HEAD AND NECK: Face > General abnormalities > Structure > Asymmetry | HP:0000324 | T0087 | |
phenodb:2941 | HEAD AND NECK: Face > General abnormalities > Structure > Broad | HP:0100729 | T0097 | |
phenodb:3636 | HEAD AND NECK: Face > General abnormalities > Structure > Cleft | HP:0002006 | T0165 | |
phenodb:3637 | HEAD AND NECK: Face > General abnormalities > Structure > Cleft > Midline | HP:0100629 | T0168 | |
phenodb:3638 | HEAD AND NECK: Face > General abnormalities > Structure > Cleft > Lateral | HP:0100731 | T0169 | |
phenodb:0142 | HEAD AND NECK: Face > General abnormalities > Structure > Coarse | HP:0000280 | T0100 | 39ff7c97ca920a5d |
phenodb:2943 | HEAD AND NECK: Face > General abnormalities > Structure > Dysmorphism | HP:0001999 | T0084 | |
phenodb:2944 | HEAD AND NECK: Face > General abnormalities > Structure > Facial hemiatrophy | HP:0011331 | T0111 | |
phenodb:2945 | HEAD AND NECK: Face > General abnormalities > Structure > Facial hemihypertophy | HP:0005323 | T0112 | |
phenodb:2942 | HEAD AND NECK: Face > General abnormalities > Structure > Facial hyperostosis | HP:0005465 | T0080 | |
phenodb:0143 | HEAD AND NECK: Face > General abnormalities > Structure > Flat | HP:0012368 | T0098 | e19b32be420aa391 |
phenodb:0144 | HEAD AND NECK: Face > General abnormalities > Structure > Long | HP:0000276 | T0094 | 811c4c37ac5a130b |
phenodb:0145 | HEAD AND NECK: Face > General abnormalities > Structure > Narrow | HP:0000275 | T0096 | 1060dfda8a77d225 |
phenodb:0146 | HEAD AND NECK: Face > General abnormalities > Structure > Prematurely aged | HP:0005328 | T0082 | fc319ee78ad21973 |
phenodb:0147 | HEAD AND NECK: Face > General abnormalities > Structure > Round | HP:0000311 | T0095 | a98d48239172dc71 |
phenodb:0148 | HEAD AND NECK: Face > General abnormalities > Structure > Short | HP:0011219 | T0093 | 2ef090892b56eb46 |
phenodb:0149 | HEAD AND NECK: Face > General abnormalities > Structure > Small | HP:0000274 | 1fdc702bb7e103ee | |
phenodb:0150 | HEAD AND NECK: Face > General abnormalities > Structure > Triangular | HP:0000325 | T0099 | 6f437512a502776b |
phenodb:0151 | HEAD AND NECK: Face > General abnormalities > Structure > Other feature | |||
phenodb:0152 | HEAD AND NECK: Face > General abnormalities > Function | |||
phenodb:0153 | HEAD AND NECK: Face > General abnormalities > Function > Dystonia | HP:0001332 | ||
phenodb:0154 | HEAD AND NECK: Face > General abnormalities > Function > Expressionless | HP:0000338 | T0102 | a721679fe5a27645 |
phenodb:0155 | HEAD AND NECK: Face > General abnormalities > Function > Hypotonic | HP:0000297 | ada1c15be8b6ddc9 | |
phenodb:0156 | HEAD AND NECK: Face > General abnormalities > Function > Palsy | HP:0010628 | ||
phenodb:0157 | HEAD AND NECK: Face > General abnormalities > Function > Palsy > Unilateral | HP:0012799 | ||
phenodb:0158 | HEAD AND NECK: Face > General abnormalities > Function > Palsy > Bilateral | HP:0001349 | ||
phenodb:0159 | HEAD AND NECK: Face > General abnormalities > Function > Paralysis | HP:0003470 | ||
phenodb:0160 | HEAD AND NECK: Face > General abnormalities > Function > Weakness | HP:0001324 | ||
phenodb:2868 | HEAD AND NECK: Face > General abnormalities > Function > Other feature | |||
phenodb:0161 | HEAD AND NECK: Face > Forehead | HP:0000290 | T0068 | |
phenodb:0162 | HEAD AND NECK: Face > Forehead > Bossing | HP:0002007 | T0070 | a223995bdef3e8d6 |
phenodb:0163 | HEAD AND NECK: Face > Forehead > Broad | HP:0000337 | T0074 | e27b1d4633855d08 |
phenodb:0164 | HEAD AND NECK: Face > Forehead > Creases, vertical | HP:0011221 | T0083 | |
phenodb:3639 | HEAD AND NECK: Face > Forehead > Glabella, prominent | HP:0002057 | T0069 | |
phenodb:2946 | HEAD AND NECK: Face > Forehead > High | HP:0000348 | T0072 | |
phenodb:0165 | HEAD AND NECK: Face > Forehead > Narrow | HP:0000341 | T0075 | 03f02219fe5521b4 |
phenodb:0166 | HEAD AND NECK: Face > Forehead > Prominent | HP:0011220 | T0071 | 510a51e4083c1d6f |
phenodb:0167 | HEAD AND NECK: Face > Forehead > Sloping | HP:0000340 | T0073 | 913a7d5a25c24e6a |
phenodb:0168 | HEAD AND NECK: Face > Forehead > Other feature | |||
phenodb:0169 | HEAD AND NECK: Face > Supraorbital region | HP:0100538 | ||
phenodb:0170 | HEAD AND NECK: Face > Supraorbital region > Prominent | HP:0000336 | T0119 | 16234cebbb88b8c2 |
phenodb:0171 | HEAD AND NECK: Face > Supraorbital region > Ridging | HP:0000336 | ||
phenodb:0172 | HEAD AND NECK: Face > Supraorbital region > Underdeveloped | HP:0009891 | T0120 | c86a7dfe73086e4e |
phenodb:0173 | HEAD AND NECK: Face > Supraorbital region > Other feature | |||
phenodb:0174 | HEAD AND NECK: Face > Midface | HP:0000309 | T0123 | |
phenodb:0175 | HEAD AND NECK: Face > Midface > Cheeks | HP:0004426 | ||
phenodb:0176 | HEAD AND NECK: Face > Midface > Cheeks > Cheekbones, prominent | HP:0012370 | 602d9b30a3a57990 | |
phenodb:0177 | HEAD AND NECK: Face > Midface > Cheeks > Cheekbones, underdeveloped | HP:0010669 | T0136 | 117a77a280a4130c |
phenodb:0178 | HEAD AND NECK: Face > Midface > Cheeks > Full | HP:0000293 | T0104 | 265070c5a30104ac |
phenodb:0179 | HEAD AND NECK: Face > Midface > Cheeks > Sunken | HP:0009938 | T0126 | |
phenodb:2947 | HEAD AND NECK: Face > Midface > Cheeks > Tags | |||
phenodb:0180 | HEAD AND NECK: Face > Midface > Cheeks > Other feature | |||
phenodb:0181 | HEAD AND NECK: Face > Midface > General abnormalities | HP:0000309 | ||
phenodb:0182 | HEAD AND NECK: Face > Midface > General abnormalities > Hypoplasia | HP:0000272 | ||
phenodb:0183 | HEAD AND NECK: Face > Midface > General abnormalities > Prominence | HP:0010620 | ||
phenodb:0184 | HEAD AND NECK: Face > Midface > General abnormalities > Retrusion | HP:0011800 | T0124 | |
phenodb:0185 | HEAD AND NECK: Face > Midface > General abnormalities > Other feature | |||
phenodb:0186 | HEAD AND NECK: Face > Midface > Hypoplasia | HP:0009117 | ||
phenodb:0187 | HEAD AND NECK: Face > Midface > Malar | HP:0012369 | T0130 | |
phenodb:0188 | HEAD AND NECK: Face > Midface > Malar > Flattening | HP:0000272 | T0134 | 81db216382f501fc |
phenodb:0189 | HEAD AND NECK: Face > Midface > Malar > Prominence | HP:0010620 | T0133 | 47d71c3912db226b |
phenodb:0190 | HEAD AND NECK: Face > Midface > Malar > Other feature | |||
phenodb:3602 | HEAD AND NECK: Face > Maxilla | HP:0000326 | T0141 | |
phenodb:3604 | HEAD AND NECK: Face > Maxilla > Asymmetry | HP:0010755 | T0142 | |
phenodb:3603 | HEAD AND NECK: Face > Maxilla > Hypoplasia | HP:0000327 | T0144 | |
phenodb:0191 | HEAD AND NECK: Face > Maxilla > Prominence | HP:0012371 | T0127 | 5f9be10c45404a8e |
phenodb:0192 | HEAD AND NECK: Face > Maxilla > Retrusion | HP:0011800 | 5b7ad34ab35682b5 | |
phenodb:3605 | HEAD AND NECK: Face > Maxilla > Other feature | |||
phenodb:0193 | HEAD AND NECK: Face > Premaxilla | HP:0010758 | ||
phenodb:3606 | HEAD AND NECK: Face > Premaxilla > Hypoplasia | HP:0010756 | ||
phenodb:0194 | HEAD AND NECK: Face > Premaxilla > Prominence | HP:0010759 | T0139 | 70623e4ed8339bf7 |
phenodb:0195 | HEAD AND NECK: Face > Premaxilla > Underdevelopment | HP:0010650 | T0140 | 7180b5fd118178e6 |
phenodb:0196 | HEAD AND NECK: Face > Premaxilla > Other feature | T0146 | ||
phenodb:0197 | HEAD AND NECK: Face > Mandible | HP:0000277 | ||
phenodb:2949 | HEAD AND NECK: Face > Mandible > Aplasia | HP:0009939 | T0148 | |
phenodb:2950 | HEAD AND NECK: Face > Mandible > Asymmetry | HP:0009940 | T0149 | |
phenodb:0198 | HEAD AND NECK: Face > Mandible > Broad | HP:0011822 | afddaffc36a1ecda | |
phenodb:0199 | HEAD AND NECK: Face > Mandible > Cleft | HP:0010752 | c06630515fcd3211 | |
phenodb:2948 | HEAD AND NECK: Face > Mandible > Hypoplasia | HP:0009118 | ||
phenodb:0200 | HEAD AND NECK: Face > Mandible > Micrognathia | HP:0000347 | T0155 | 8bbf61b4ad7ca2ef |
phenodb:0201 | HEAD AND NECK: Face > Mandible > Narrow | HP:0012801 | 4e6212887b3f3f6a | |
phenodb:0202 | HEAD AND NECK: Face > Mandible > Prognathism | HP:0000303 | cf3eb35245d52feb | |
phenodb:0203 | HEAD AND NECK: Face > Mandible > Retrognathia | HP:0000278 | T0154 | 588f04d3f1b40b25 |
phenodb:0204 | HEAD AND NECK: Face > Mandible > Other feature | |||
phenodb:0205 | HEAD AND NECK: Face > Chin | HP:0000306 | T0150 | |
phenodb:0206 | HEAD AND NECK: Face > Chin > Broad | HP:0011822 | T0151 | 0f587b4c5715c846 |
phenodb:0207 | HEAD AND NECK: Face > Chin > Crease(s) | HP:0011823 | ||
phenodb:0208 | HEAD AND NECK: Face > Chin > Dimple | HP:0010751 | T0157 | bc5eac0c32d427f2 |
phenodb:0209 | HEAD AND NECK: Face > Chin > Pointed | HP:0000307 | T0158 | 7c4085d40e70f0c9 |
phenodb:0210 | HEAD AND NECK: Face > Chin > Prominent | HP:0000303 | T0152 | |
phenodb:0211 | HEAD AND NECK: Face > Chin > Short | HP:0000331 | T0156 | 2fd642c0ef7883ca |
phenodb:0212 | HEAD AND NECK: Face > Chin > Other feature | HP:0000347 | ||
phenodb:0213 | HEAD AND NECK: Eyes | |||
phenodb:0214 | HEAD AND NECK: Eyes > Function | HP:0012373 | ||
phenodb:0215 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles | HP:0000496 | ||
phenodb:0216 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles > Abnormal eye movements | HP:0000496 | T0326 | |
phenodb:0217 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles > Astigmatism | HP:0000483 | T0319 | |
phenodb:0218 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles > Blepharospasm | HP:0000643 | T2215 | |
phenodb:0219 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles > Congenital fibrosis of the extraocular muscles (CFEOM) | HP:0001491 | T0329 | |
phenodb:0220 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles > Duane anomaly | HP:0009921 | T0327 | |
phenodb:0221 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles > Dysmetric saccades | HP:0000641 | T0328 | |
phenodb:0222 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles > External ophthalmoplegia (aka Chronic progressive external ophthalmoplegia / CPEO) | HP:0000544 | T0340 | |
phenodb:0223 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles > Impaired smooth pursuit | HP:0007772 | T0343 | |
phenodb:0224 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles > Nystagmus | HP:0000639 | ||
phenodb:0225 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles > Nystagmus > Horizontal | HP:0000666 | T0335 | |
phenodb:2951 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles > Nystagmus > Pendular | HP:0012043 | T0336 | |
phenodb:0226 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles > Nystagmus > Rotatory | HP:0001583 | T0338 | |
phenodb:0227 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles > Nystagmus > Vertical | HP:0010544 | T0337 | |
phenodb:0228 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles > Nystagmus > Other feature | |||
phenodb:0229 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles > Oculogyric crisis | HP:0010553 | ||
phenodb:0230 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles > Oculomotor apraxia | HP:0000657 | T0342 | |
phenodb:0231 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles > Ophthalmoparesis | HP:0000597 | ||
phenodb:0232 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles > Ophthalmoplegia | HP:0000602 | T0339 | |
phenodb:0233 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles > Ophthalmoplegia, supranuclear | HP:0000623 | T0341 | |
phenodb:0234 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles > Slow saccades | HP:0000514 | T0330 | |
phenodb:0235 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles > Strabismus | HP:0000486 | T0331 | |
phenodb:0236 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles > Strabismus > Esotropia | HP:0000565 | T0333 | |
phenodb:0237 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles > Strabismus > Exotropia | HP:0000577 | T0332 | |
phenodb:0238 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles > Strabismus > Other feature | |||
phenodb:2869 | HEAD AND NECK: Eyes > Function > Globe movements & extra-ocular muscles > Other feature | |||
phenodb:0239 | HEAD AND NECK: Eyes > Function > Vision | HP:0000504 | T0296 | |
phenodb:0240 | HEAD AND NECK: Eyes > Function > Vision > Abnormal electroretinogram (aka Abnormal ERG) | HP:0000512 | T0322 | |
phenodb:0241 | HEAD AND NECK: Eyes > Function > Vision > Abnormal visual evoked response (aka Abnormal VER; VECP) | HP:0000649 | T0323 | |
phenodb:0245 | HEAD AND NECK: Eyes > Function > Vision > Alacrima | HP:0000522 | T0244 | |
phenodb:2952 | HEAD AND NECK: Eyes > Function > Vision > Amaurosis fugax | HP:0100576 | T0305 | |
phenodb:0242 | HEAD AND NECK: Eyes > Function > Vision > Amblyopia | HP:0000646 | T0302 | |
phenodb:0243 | HEAD AND NECK: Eyes > Function > Vision > Anisometropic | HP:0012803 | ||
phenodb:0246 | HEAD AND NECK: Eyes > Function > Vision > Blindness | HP:0000618 | T0303 | |
phenodb:0247 | HEAD AND NECK: Eyes > Function > Vision > Blindness, cortical (aka Cerebral visual impairment) | HP:0100704 | ||
phenodb:0248 | HEAD AND NECK: Eyes > Function > Vision > Blurred vision | HP:0000622 | T0301 | |
phenodb:0249 | HEAD AND NECK: Eyes > Function > Vision > Central scotoma | HP:0000603 | T0298 | |
phenodb:2953 | HEAD AND NECK: Eyes > Function > Vision > Day blindness | HP:0012047 | ||
phenodb:0250 | HEAD AND NECK: Eyes > Function > Vision > Decreased visual acuity | HP:0000505 | T0308 | |
phenodb:0251 | HEAD AND NECK: Eyes > Function > Vision > Diplopia | HP:0000651 | T0320 | |
phenodb:0252 | HEAD AND NECK: Eyes > Function > Vision > Dyschromatopsia (aka Colorblindness) | HP:0007641 | T0310 | |
phenodb:0253 | HEAD AND NECK: Eyes > Function > Vision > Dyschromatopsia (aka Colorblindness) > Blue | HP:0000552 | T0314 | |
phenodb:0254 | HEAD AND NECK: Eyes > Function > Vision > Dyschromatopsia (aka Colorblindness) > Red | HP:0000642 | T0311 | |
phenodb:0255 | HEAD AND NECK: Eyes > Function > Vision > Dyschromatopsia (aka Colorblindness) > Green | HP:0000642 | ||
phenodb:0256 | HEAD AND NECK: Eyes > Function > Vision > Dyschromatopsia (aka Colorblindness) > Other feature | |||
phenodb:2954 | HEAD AND NECK: Eyes > Function > Vision > Hemianopsia | HP:0012377 | T0325 | |
phenodb:0244 | HEAD AND NECK: Eyes > Function > Vision > Hypermetropic | HP:0000540 | ||
phenodb:0257 | HEAD AND NECK: Eyes > Function > Vision > Hypermetropia | HP:0000540 | T0316 | |
phenodb:0258 | HEAD AND NECK: Eyes > Function > Vision > Hyperopia | HP:0000540 | ||
phenodb:0259 | HEAD AND NECK: Eyes > Function > Vision > Myopia | HP:0000545 | T0317 | |
phenodb:0260 | HEAD AND NECK: Eyes > Function > Vision > Myopia > High | HP:0011003 | T0318 | |
phenodb:0261 | HEAD AND NECK: Eyes > Function > Vision > Myopia > Other feature | |||
phenodb:0262 | HEAD AND NECK: Eyes > Function > Vision > Night blindness | HP:0000662 | T0307 | |
phenodb:0263 | HEAD AND NECK: Eyes > Function > Vision > Peripheral vision loss (aka Tunnel vision) | HP:0007994 | ||
phenodb:0265 | HEAD AND NECK: Eyes > Function > Vision > Photodysphoria | HP:0000613 | ||
phenodb:0264 | HEAD AND NECK: Eyes > Function > Vision > Photophobia | HP:0000613 | ||
phenodb:0266 | HEAD AND NECK: Eyes > Function > Vision > Photosternutation (aka Photic sneezing) | |||
phenodb:0267 | HEAD AND NECK: Eyes > Function > Vision > Progressive visual loss | HP:0000529 | T0304 | |
phenodb:0268 | HEAD AND NECK: Eyes > Function > Vision > Visual field loss | HP:0001123 | T0324 | |
phenodb:2870 | HEAD AND NECK: Eyes > Function > Vision > Other feature | |||
phenodb:0269 | HEAD AND NECK: Eyes > Structure | HP:0012372 | ||
phenodb:0270 | HEAD AND NECK: Eyes > Structure > General (globe) | HP:0012374 | ||
phenodb:0271 | HEAD AND NECK: Eyes > Structure > General (globe) > Anophthalmos / Anophthalmia | HP:0000528 | T0181 | |
phenodb:2955 | HEAD AND NECK: Eyes > Structure > General (globe) > Buphthalmos | HP:0000557 | T0185 | |
phenodb:2956 | HEAD AND NECK: Eyes > Structure > General (globe) > Cyclopia | HP:0009914 | T0186 | |
phenodb:0272 | HEAD AND NECK: Eyes > Structure > General (globe) > Keratoconus | HP:0000563 | T0235 | |
phenodb:0273 | HEAD AND NECK: Eyes > Structure > General (globe) > Microphthalmos / Microphthalmia | HP:0000568 | T0182 | |
phenodb:0274 | HEAD AND NECK: Eyes > Structure > General (globe) > Phthisis bulbi | HP:0000667 | T0173 | |
phenodb:2957 | HEAD AND NECK: Eyes > Structure > General (globe) > Spontaneous rupture of globe | HP:0010727 | T0188 | |
phenodb:0275 | HEAD AND NECK: Eyes > Structure > General (globe) > Other feature | |||
phenodb:0276 | HEAD AND NECK: Eyes > Structure > Anterior chamber | HP:0000593 | T0198 | |
phenodb:0277 | HEAD AND NECK: Eyes > Structure > Anterior chamber > Axenfeld anomaly | HP:0001492 | ||
phenodb:0278 | HEAD AND NECK: Eyes > Structure > Anterior chamber > Axenfeld-Reiger anomaly | HP:0001492 | T0217 | |
phenodb:0279 | HEAD AND NECK: Eyes > Structure > Anterior chamber > Band keratopathy | HP:0000585 | T0220 | |
phenodb:0280 | HEAD AND NECK: Eyes > Structure > Anterior chamber > Posterior embryotoxon | HP:0000627 | T0216 | |
phenodb:0281 | HEAD AND NECK: Eyes > Structure > Anterior chamber > Rieger anomaly | HP:0000558 | T0199 | |
phenodb:0282 | HEAD AND NECK: Eyes > Structure > Anterior chamber > Other feature | |||
phenodb:3640 | HEAD AND NECK: Eyes > Structure > Choroid | HP:0000610 | T0262 | |
phenodb:3641 | HEAD AND NECK: Eyes > Structure > Conjunctiva | HP:0000502 | T0212 | |
phenodb:3642 | HEAD AND NECK: Eyes > Structure > Conjunctiva > Conjunctivitis | HP:0000509 | T0239 | |
phenodb:3643 | HEAD AND NECK: Eyes > Structure > Conjunctiva > Xerophthalmia | HP:0001097 | T0245 | |
phenodb:3644 | HEAD AND NECK: Eyes > Structure > Conjunctiva > Telangiectasia | HP:0000524 | T0248 | |
phenodb:0283 | HEAD AND NECK: Eyes > Structure > Cornea | HP:0000481 | T0219 | |
phenodb:3645 | HEAD AND NECK: Eyes > Structure > Cornea > Corneal arcus | HP:0001084 | T0233 | |
phenodb:0284 | HEAD AND NECK: Eyes > Structure > Cornea > Clouding | HP:0007957 | ||
phenodb:3646 | HEAD AND NECK: Eyes > Structure > Cornea > Dystrophy | HP:0001131 | T0230 | |
phenodb:0285 | HEAD AND NECK: Eyes > Structure > Cornea > Erosions | HP:0200020 | ||
phenodb:0286 | HEAD AND NECK: Eyes > Structure > Cornea > Megalocornea | HP:0000485 | T0227 | |
phenodb:0287 | HEAD AND NECK: Eyes > Structure > Cornea > Microcornea | HP:0000482 | T0226 | |
phenodb:0288 | HEAD AND NECK: Eyes > Structure > Cornea > Opacity | HP:0007957 | T0223 | |
phenodb:3647 | HEAD AND NECK: Eyes > Structure > Cornea > Plana | HP:0007720 | T0228 | |
phenodb:0289 | HEAD AND NECK: Eyes > Structure > Cornea > Sclerocornea | HP:0000647 | ||
phenodb:0290 | HEAD AND NECK: Eyes > Structure > Cornea > Ulceration | HP:0012804 | T0224 | |
phenodb:0291 | HEAD AND NECK: Eyes > Structure > Cornea > Other feature | |||
phenodb:0292 | HEAD AND NECK: Eyes > Structure > Lens | HP:0000517 | ||
phenodb:0293 | HEAD AND NECK: Eyes > Structure > Lens > Cataract | HP:0000518 | T0249 | |
phenodb:0294 | HEAD AND NECK: Eyes > Structure > Lens > Cataract > Congenital | HP:0000519 | T0252 | |
phenodb:0295 | HEAD AND NECK: Eyes > Structure > Lens > Cataract > Cortical | HP:0100019 | ||
phenodb:0296 | HEAD AND NECK: Eyes > Structure > Lens > Cataract > Nuclear | HP:0100018 | ||
phenodb:0297 | HEAD AND NECK: Eyes > Structure > Lens > Cataract > Total | HP:0010700 | ||
phenodb:0298 | HEAD AND NECK: Eyes > Structure > Lens > Cataract > Other feature | |||
phenodb:0299 | HEAD AND NECK: Eyes > Structure > Lens > Ectopia lentis | HP:0001083 | T0255 | |
phenodb:3648 | HEAD AND NECK: Eyes > Structure > Lens > Shape | HP:0011526 | T0259 | |
phenodb:3649 | HEAD AND NECK: Eyes > Structure > Lens > Shape > Lenticonus | HP:0011527 | T0257 | |
phenodb:0300 | HEAD AND NECK: Eyes > Structure > Lens > Microphakia | HP:0012376 | T0256 | |
phenodb:2871 | HEAD AND NECK: Eyes > Structure > Lens > Other feature | |||
phenodb:0301 | HEAD AND NECK: Eyes > Structure > Epibulbar dermoids | HP:0001140 | T0247 | |
phenodb:0302 | HEAD AND NECK: Eyes > Structure > Glaucoma | HP:0000501 | T0183 | |
phenodb:0303 | HEAD AND NECK: Eyes > Structure > Glaucoma > Congenital (aka bupthalmos) | HP:0001087 | ||
phenodb:0304 | HEAD AND NECK: Eyes > Structure > Glaucoma > Other feature | |||
phenodb:0305 | HEAD AND NECK: Eyes > Structure > Iris | HP:0000525 | T0200 | |
phenodb:0306 | HEAD AND NECK: Eyes > Structure > Iris > Absent / Aniridia | HP:0000526 | T0204 | |
phenodb:0307 | HEAD AND NECK: Eyes > Structure > Iris > Bright blue | HP:0000635 | ||
phenodb:0308 | HEAD AND NECK: Eyes > Structure > Iris > Coloboma | HP:0000612 | T0205 | |
phenodb:3650 | HEAD AND NECK: Eyes > Structure > Iris > Depigmentation | HP:0007730 | T0201 | |
phenodb:0309 | HEAD AND NECK: Eyes > Structure > Iris > Hypoplasia | HP:0007676 | T0203 | |
phenodb:0310 | HEAD AND NECK: Eyes > Structure > Iris > Heterochromia | HP:0001100 | T0206 | |
phenodb:0311 | HEAD AND NECK: Eyes > Structure > Iris > Lisch nodules | HP:0009737 | ||
phenodb:0312 | HEAD AND NECK: Eyes > Structure > Iris > Stellate | HP:0012775 | ||
phenodb:0313 | HEAD AND NECK: Eyes > Structure > Iris > Transillumination | HP:0012805 | ||
phenodb:0314 | HEAD AND NECK: Eyes > Structure > Iris > Other feature | |||
phenodb:0315 | HEAD AND NECK: Eyes > Structure > Increased intraocular pressure | HP:0007906 | T2894 | |
phenodb:0316 | HEAD AND NECK: Eyes > Structure > Keratitis | HP:0000491 | T0240 | |
phenodb:3651 | HEAD AND NECK: Eyes > Structure > Pupil | HP:0000615 | T0189 | |
phenodb:3652 | HEAD AND NECK: Eyes > Structure > Pupil > Asymmetric | HP:0009916 | T0196 | |
phenodb:3653 | HEAD AND NECK: Eyes > Structure > Pupil > Constricted | HP:0000616 | T0190 | |
phenodb:3654 | HEAD AND NECK: Eyes > Structure > Pupil > Dilated | HP:0011499 | T0192 | |
phenodb:3655 | HEAD AND NECK: Eyes > Structure > Pupil > Ectopic | HP:0009918 | T0195 | |
phenodb:3656 | HEAD AND NECK: Eyes > Structure > Pupil > Persistent pupillary membrane | HP:0009917 | T0194 | |
phenodb:3657 | HEAD AND NECK: Eyes > Structure > Pupil > Tonic | HP:0012074 | T0191 | |
phenodb:0317 | HEAD AND NECK: Eyes > Structure > Peters anomaly | HP:0000659 | T0174 | |
phenodb:3658 | HEAD AND NECK: Eyes > Structure > Sclerae | HP:0000591 | T0215 | |
phenodb:3659 | HEAD AND NECK: Eyes > Structure > Sclerae > Scleritis | HP:0100532 | T0241 | |
phenodb:0318 | HEAD AND NECK: Eyes > Structure > Sclerae > Blue | HP:0000592 | T0238 | |
phenodb:0319 | HEAD AND NECK: Eyes > Structure > Telangectasia of the conjunctiva | HP:0000524 | ||
phenodb:0320 | HEAD AND NECK: Eyes > Structure > Uveitits | HP:0000554 | T0242 | |
phenodb:0321 | HEAD AND NECK: Eyes > Structure > Vitreous | HP:0004327 | T0263 | |
phenodb:0322 | HEAD AND NECK: Eyes > Structure > Vitreous > Vitreoretinal degeneration | HP:0000655 | T0214 | |
phenodb:0323 | HEAD AND NECK: Eyes > Structure > Vitreous > Vitreous hemorrhage | HP:0007902 | T0267 | |
phenodb:3660 | HEAD AND NECK: Eyes > Structure > Vitreous > Vitreous floaters | HP:0100832 | T0270 | |
phenodb:3661 | HEAD AND NECK: Eyes > Structure > Vitreous > Vitritis | HP:0011531 | T0264 | |
phenodb:3662 | HEAD AND NECK: Eyes > Structure > Vitreous > Persistent primary vitreous | HP:0007968 | T0265 | |
phenodb:0324 | HEAD AND NECK: Eyes > Structure > Vitreous > Other feature | |||
phenodb:0325 | HEAD AND NECK: Eyes > Structure > Optic nerve | HP:0000587 | ||
phenodb:0326 | HEAD AND NECK: Eyes > Structure > Optic nerve > Atrophy | HP:0000648 | ||
phenodb:2958 | HEAD AND NECK: Eyes > Structure > Optic nerve > Coloboma | HP:0000588 | T0295 | |
phenodb:0327 | HEAD AND NECK: Eyes > Structure > Optic nerve > Hypoplasia | HP:0000609 | T0291 | |
phenodb:0328 | HEAD AND NECK: Eyes > Structure > Optic nerve > Pallor | HP:0000543 | T0294 | |
phenodb:0329 | HEAD AND NECK: Eyes > Structure > Optic nerve > Pit | HP:0012796 | ||
phenodb:0330 | HEAD AND NECK: Eyes > Structure > Optic nerve > Glioma | HP:0009733 | ||
phenodb:0331 | HEAD AND NECK: Eyes > Structure > Optic nerve > Papilledema | HP:0001085 | T0290 | |
phenodb:0332 | HEAD AND NECK: Eyes > Structure > Optic nerve > Pseudopapilledema | HP:0000538 | ||
phenodb:0333 | HEAD AND NECK: Eyes > Structure > Optic nerve > Other feature | |||
phenodb:0334 | HEAD AND NECK: Eyes > Structure > Retina | HP:0000479 | T0176 | |
phenodb:3663 | HEAD AND NECK: Eyes > Structure > Retina > Chorioretinal dystrophy | HP:0007731 | T0284 | |
phenodb:0335 | HEAD AND NECK: Eyes > Structure > Retina > Chorioretinal lacunae | HP:0007858 | T0281 | |
phenodb:0336 | HEAD AND NECK: Eyes > Structure > Retina > Coloboma | HP:0000567 | T0268 | |
phenodb:0337 | HEAD AND NECK: Eyes > Structure > Retina > Degeneration | HP:0000546 | T0280 | |
phenodb:0338 | HEAD AND NECK: Eyes > Structure > Retina > Detachment | HP:0000541 | T0271 | |
phenodb:0339 | HEAD AND NECK: Eyes > Structure > Retina > Dystrophy | HP:0000556 | T2898 | |
phenodb:3664 | HEAD AND NECK: Eyes > Structure > Retina > Hamartoma | HP:0009594 | T0276 | |
phenodb:0340 | HEAD AND NECK: Eyes > Structure > Retina > Hemorrhage | HP:0000573 | T0179 | |
phenodb:0341 | HEAD AND NECK: Eyes > Structure > Retina > Hypopigmentation (Pallor) | HP:0001010 | ||
phenodb:2959 | HEAD AND NECK: Eyes > Structure > Retina > Anomaly of the macula | HP:0001103 | T0178 | |
phenodb:0342 | HEAD AND NECK: Eyes > Structure > Retina > Macular cherry red spot | HP:0010729 | ||
phenodb:3665 | HEAD AND NECK: Eyes > Structure > Retina > Macular coloboma | HP:0011511 | T0277 | |
phenodb:0343 | HEAD AND NECK: Eyes > Structure > Retina > Macular degeneration | HP:0000608 | T0266 | |
phenodb:2960 | HEAD AND NECK: Eyes > Structure > Retina > Macular dystophy | HP:0007754 | T0287 | |
phenodb:0344 | HEAD AND NECK: Eyes > Structure > Retina > Macular hypoplasia | HP:0001104 | ||
phenodb:3666 | HEAD AND NECK: Eyes > Structure > Retina > Macular pigment anomaly | HP:0008002 | T0274 | |
phenodb:0345 | HEAD AND NECK: Eyes > Structure > Retina > Miosis | HP:0000616 | ||
phenodb:0346 | HEAD AND NECK: Eyes > Structure > Retina > Ocular albinism | HP:0001107 | ||
phenodb:0347 | HEAD AND NECK: Eyes > Structure > Retina > Pigmentary retinopathy | HP:0000580 | T0282 | |
phenodb:0348 | HEAD AND NECK: Eyes > Structure > Retina > Retinal artery tortuosity | HP:0000631 | T0273 | |
phenodb:0349 | HEAD AND NECK: Eyes > Structure > Retina > Retinitis pigmentosa | HP:0000510 | ||
phenodb:0350 | HEAD AND NECK: Eyes > Structure > Retina > Retinopathy | HP:0000488 | T0279 | |
phenodb:3667 | HEAD AND NECK: Eyes > Structure > Retina > Telangiectasia | HP:0007763 | T0272 | |
phenodb:0351 | HEAD AND NECK: Eyes > Structure > Retina > Other feature | |||
phenodb:0352 | HEAD AND NECK: Periorbital region | HP:0000606 | ||
phenodb:0353 | HEAD AND NECK: Periorbital region > Shape / Position / Spacing | |||
phenodb:0354 | HEAD AND NECK: Periorbital region > Shape / Position / Spacing > Almond-shaped eyes | HP:0007874 | T0089 | 5112bd7cd0e7bd8e |
phenodb:0355 | HEAD AND NECK: Periorbital region > Shape / Position / Spacing > Closely spaced eyes (aka Hypotelorism) | HP:0000601 | T0115 | 71d9f1be67c7f8b6 |
phenodb:0356 | HEAD AND NECK: Periorbital region > Shape / Position / Spacing > Deeply-set eyes (aka Sunken eyes / Enophthalmos) | HP:0000490 | T0122 | 572ee266fb56c22a |
phenodb:0357 | HEAD AND NECK: Periorbital region > Shape / Position / Spacing > Palpebral fissures | HP:0008050 | T0088 | |
phenodb:0358 | HEAD AND NECK: Periorbital region > Shape / Position / Spacing > Palpebral fissures > Downslanting | HP:0000494 | 1c4dc8688933b9ef | |
phenodb:0359 | HEAD AND NECK: Periorbital region > Shape / Position / Spacing > Palpebral fissures > Long (aka Wide) | HP:0000637 | T0386 | 7d54404e36c3ddb9 |
phenodb:0360 | HEAD AND NECK: Periorbital region > Shape / Position / Spacing > Palpebral fissures > Narrow | |||
phenodb:0361 | HEAD AND NECK: Periorbital region > Shape / Position / Spacing > Palpebral fissures > Short | HP:0012745 | T0374 | 8ea165ff88fe04c3 |
phenodb:0362 | HEAD AND NECK: Periorbital region > Shape / Position / Spacing > Palpebral fissures > Upslanting | HP:0000582 | T0117 | f103f00fcb26b7c4 |
phenodb:0363 | HEAD AND NECK: Periorbital region > Shape / Position / Spacing > Palpebral fissures > Other feature | |||
phenodb:0364 | HEAD AND NECK: Periorbital region > Shape / Position / Spacing > Proptosis (aka Prominent eyes / Exophthalmos) | HP:0000520 | T0121 | 765f49f1e824f0d2 |
phenodb:0365 | HEAD AND NECK: Periorbital region > Shape / Position / Spacing > Shallow orbits | HP:0000586 | ||
phenodb:0366 | HEAD AND NECK: Periorbital region > Shape / Position / Spacing > Widely spaced eyes (aka Hypertelorism) | HP:0000316 | T0113 | 5bfbc4ab8a8af765 |
phenodb:2872 | HEAD AND NECK: Periorbital region > Shape / Position / Spacing > Other feature | |||
phenodb:0367 | HEAD AND NECK: Periorbital region > Inner canthal region | |||
phenodb:0368 | HEAD AND NECK: Periorbital region > Inner canthal region > Epicanthal folds | HP:0000286 | T0376 | 8b4ac9cc8a79aa3e |
phenodb:0369 | HEAD AND NECK: Periorbital region > Inner canthal region > Epicanthus inversus | HP:0000537 | T0377 | d862798b5055800d |
phenodb:0370 | HEAD AND NECK: Periorbital region > Inner canthal region > Telecanthus (aka Dystopia canthorum) | HP:0000506 | T0378 | 55fb0667392bab43 |
phenodb:0371 | HEAD AND NECK: Periorbital region > Inner canthal region > Other feature | |||
phenodb:0372 | HEAD AND NECK: Periorbital region > Eyelids | HP:0000492 | T0360 | |
phenodb:0373 | HEAD AND NECK: Periorbital region > Eyelids > Ablepharon (aka Absent eyelids) | HP:0011224 | T0383 | 5dec14811ba250f8 |
phenodb:0374 | HEAD AND NECK: Periorbital region > Eyelids > Ankyloblepharon (aka Eyelid synechiae / Ankyloblepharon filiforme adnatum) | HP:0009755 | T0371 | 9aefd466e74d3204 |
phenodb:0375 | HEAD AND NECK: Periorbital region > Eyelids > Blepharochalasis (aka Wrinkled eyelids / Thin eyelids) | HP:0010749 | T0362 | 995a2398db7eefe2 |
phenodb:0376 | HEAD AND NECK: Periorbital region > Eyelids > Blepharophimosis | HP:0000581 | T0375 | 88ebc039bbbaef0f |
phenodb:2963 | HEAD AND NECK: Periorbital region > Eyelids > Chronic blepharitis | HP:0000498 | ||
phenodb:2962 | HEAD AND NECK: Periorbital region > Eyelids > Coloboma of lower eyelid | HP:0000625 | ||
phenodb:2961 | HEAD AND NECK: Periorbital region > Eyelids > Coloboma of upper eyelid | HP:0000636 | T0364 | |
phenodb:0378 | HEAD AND NECK: Periorbital region > Eyelids > Cryptophthalmos | HP:0001126 | T0370 | 339585ad3ac88686 |
phenodb:0379 | HEAD AND NECK: Periorbital region > Eyelids > Ectropion | HP:0000656 | T0381 | 49cad0d3ae6a54ac |
phenodb:0380 | HEAD AND NECK: Periorbital region > Eyelids > Entropion | HP:0000621 | T0382 | 34a546ebf02511b5 |
phenodb:0381 | HEAD AND NECK: Periorbital region > Eyelids > Epiblepharon | HP:0011225 | T0218 | 0ca0ac3d52bda364 |
phenodb:0377 | HEAD AND NECK: Periorbital region > Eyelids > Eyelid cleft (aka Eyelid coloboma / Eyelid notched) | HP:0000625 | dec367cb72e7cf0b | |
phenodb:0382 | HEAD AND NECK: Periorbital region > Eyelids > Infra-orbital crease | HP:0100876 | T0175 | |
phenodb:0383 | HEAD AND NECK: Periorbital region > Eyelids > Infra-orbital fold | HP:0011232 | T2893 | |
phenodb:2964 | HEAD AND NECK: Periorbital region > Eyelids > Lagophthalmos | |||
phenodb:2965 | HEAD AND NECK: Periorbital region > Eyelids > Periorbital edema | HP:0100539 | T0387 | |
phenodb:0384 | HEAD AND NECK: Periorbital region > Eyelids > Ptosis (aka Blepharoptosis) | HP:0000508 | T0373 | 1bd157b764ec7aea |
phenodb:0385 | HEAD AND NECK: Periorbital region > Eyelids > Upper eyelid fullness | HP:0000629 | 224e1bf4e42c7ea7 | |
phenodb:0386 | HEAD AND NECK: Periorbital region > Eyelids > Other feature | |||
phenodb:0387 | HEAD AND NECK: Periorbital region > Eyebrows | HP:0000534 | T0345 | |
phenodb:2966 | HEAD AND NECK: Periorbital region > Eyebrows > Absent | HP:0002223 | T0350 | |
phenodb:0388 | HEAD AND NECK: Periorbital region > Eyebrows > Arched | HP:0002553 | ||
phenodb:0389 | HEAD AND NECK: Periorbital region > Eyebrows > Broad (aka Flared) | HP:0000574 | b3939766d0196a62 | |
phenodb:0390 | HEAD AND NECK: Periorbital region > Eyebrows > Heavy / Bushy | HP:0000574 | 1cb59db7a74b5a73 | |
phenodb:0391 | HEAD AND NECK: Periorbital region > Eyebrows > Highly arched | HP:0002553 | T0354 | 58b4e59edca46f0a |
phenodb:0392 | HEAD AND NECK: Periorbital region > Eyebrows > Horizontal (aka Straight) | HP:0011228 | T0346 | 8cf5bb1a10ac0831 |
phenodb:2967 | HEAD AND NECK: Periorbital region > Eyebrows > Lateral thinning | HP:0005338 | T0357 | |
phenodb:0393 | HEAD AND NECK: Periorbital region > Eyebrows > Laterally extended | HP:0007933 | c8fe0ea0a0e1e73c | |
phenodb:2968 | HEAD AND NECK: Periorbital region > Eyebrows > Medial flaring | HP:0010747 | T0356 | |
phenodb:0394 | HEAD AND NECK: Periorbital region > Eyebrows > Sparse (aka Eyebrow hypotrichosis) | HP:0000535 | T0349 | e46e4f358187a32a |
phenodb:0395 | HEAD AND NECK: Periorbital region > Eyebrows > Synophrys (aka Unibrow) | HP:0000664 | T0353 | 5e417df50b2316f4 |
phenodb:0396 | HEAD AND NECK: Periorbital region > Eyebrows > Thick (aka Bushy / Eyebrow hirsutism) | HP:0000574 | T0351 | |
phenodb:0397 | HEAD AND NECK: Periorbital region > Eyebrows > White | HP:0002226 | T0347 | |
phenodb:0398 | HEAD AND NECK: Periorbital region > Eyebrows > Other feature | |||
phenodb:0399 | HEAD AND NECK: Periorbital region > Eyelashes | HP:0000499 | T0361 | |
phenodb:0400 | HEAD AND NECK: Periorbital region > Eyelashes > Absent (aka Atrichia of eyelashes) | HP:0000561 | T0392 | c509fa22bdbdd8e0 |
phenodb:2969 | HEAD AND NECK: Periorbital region > Eyelashes > Curly | HP:0007665 | T0388 | |
phenodb:0401 | HEAD AND NECK: Periorbital region > Eyelashes > Distachiasis | HP:0009743 | T0391 | |
phenodb:0402 | HEAD AND NECK: Periorbital region > Eyelashes > Long (aka Ciliary trichomegaly) | HP:0000527 | T0389 | b1145bac0932da43 |
phenodb:0403 | HEAD AND NECK: Periorbital region > Eyelashes > Prominent | HP:0011231 | f14f2e7a99834f46 | |
phenodb:0404 | HEAD AND NECK: Periorbital region > Eyelashes > Sparse (aka Atrychia and Hypotrichosis of eyelashes) | HP:0000653 | T0393 | c509fa22bdbdd8e0 |
phenodb:0405 | HEAD AND NECK: Periorbital region > Eyelashes > White | HP:0002227 | T0368 | |
phenodb:0406 | HEAD AND NECK: Periorbital region > Eyelashes > Other feature | |||
phenodb:0407 | HEAD AND NECK: Periorbital region > Lacrimal system | HP:0000614 | T0394 | |
phenodb:0408 | HEAD AND NECK: Periorbital region > Lacrimal system > Lacrimal duct obstruction | HP:0000579 | T0365 | |
phenodb:2970 | HEAD AND NECK: Periorbital region > Lacrimal system > Increased lacrimation | HP:0009926 | T0398 | |
phenodb:0409 | HEAD AND NECK: Periorbital region > Lacrimal system > Lacrimal punctum | HP:0011479 | ||
phenodb:0410 | HEAD AND NECK: Periorbital region > Lacrimal system > Lacrimal punctum > Absent (aka Agenesis of lacrimal punctum) | HP:0001092 | T0367 | 479ccad9356835fd |
phenodb:0411 | HEAD AND NECK: Periorbital region > Lacrimal system > Lacrimal punctum > Ectopic | HP:0010748 | T0396 | fc20192af0b38fd3 |
phenodb:0412 | HEAD AND NECK: Periorbital region > Lacrimal system > Lacrimal punctum > Other feature | |||
phenodb:0413 | HEAD AND NECK: Ears / Hearing | HP:0000364 | ||
phenodb:0414 | HEAD AND NECK: Ears / Hearing > Structure | HP:0000598 | T0618 | |
phenodb:0415 | HEAD AND NECK: Ears / Hearing > Structure > General / Position | HP:0000357 | ||
phenodb:0416 | HEAD AND NECK: Ears / Hearing > Structure > General / Position > Anotia | HP:0009892 | T0640 | 8b2ea8525fbaf767 |
phenodb:0417 | HEAD AND NECK: Ears / Hearing > Structure > General / Position > Asymmetric size | HP:0010722 | T0620 | |
phenodb:0418 | HEAD AND NECK: Ears / Hearing > Structure > General / Position > Calcified | HP:0005103 | ||
phenodb:2971 | HEAD AND NECK: Ears / Hearing > Structure > General / Position > Cryptotia | HP:0011252 | T0639 | |
phenodb:0438 | HEAD AND NECK: Ears / Hearing > Structure > General / Position > Dysplastic / Malformed ears | HP:0008572 | T0624 | |
phenodb:0439 | HEAD AND NECK: Ears / Hearing > Structure > General / Position > Large | HP:0000400 | T0644 | |
phenodb:0440 | HEAD AND NECK: Ears / Hearing > Structure > General / Position > Lop | HP:0000394 | T0630 | b03dbc6169755a51 |
phenodb:0419 | HEAD AND NECK: Ears / Hearing > Structure > General / Position > Low set | HP:0000369 | T0636 | |
phenodb:0420 | HEAD AND NECK: Ears / Hearing > Structure > General / Position > Microtia | HP:0008551 | T0638 | |
phenodb:0421 | HEAD AND NECK: Ears / Hearing > Structure > General / Position > Otitis media, chronic | HP:0000389 | T0724 | |
phenodb:0422 | HEAD AND NECK: Ears / Hearing > Structure > General / Position > Otosclerosis | HP:0000362 | T0623 | |
phenodb:0424 | HEAD AND NECK: Ears / Hearing > Structure > General / Position > Pit - postauricular | HP:0004464 | T0659 | |
phenodb:0423 | HEAD AND NECK: Ears / Hearing > Structure > General / Position > Pit - preauricular | HP:0004467 | T0621 | 792cfeacf93ca391 |
phenodb:0425 | HEAD AND NECK: Ears / Hearing > Structure > General / Position > Posteriorly rotated | HP:0000358 | T0635 | d6850b6df27359e2 |
phenodb:2972 | HEAD AND NECK: Ears / Hearing > Structure > General / Position > Preauricular fistula | |||
phenodb:2973 | HEAD AND NECK: Ears / Hearing > Structure > General / Position > Pretragal ectopia | HP:0030024 | T0642 | |
phenodb:0426 | HEAD AND NECK: Ears / Hearing > Structure > General / Position > Prominent / Protruding | HP:0000411 | T0637 | 2dfb8b544358ccda |
phenodb:2974 | HEAD AND NECK: Ears / Hearing > Structure > General / Position > Synotia | HP:0100663 | T0643 | |
phenodb:0428 | HEAD AND NECK: Ears / Hearing > Structure > General / Position > Tag - postauricular | HP:0004451 | T0701 | |
phenodb:0427 | HEAD AND NECK: Ears / Hearing > Structure > General / Position > Tag - preauricular | HP:0000384 | T0700 | f970afa16e397ece |
phenodb:0429 | HEAD AND NECK: Ears / Hearing > Structure > External ear | |||
phenodb:0430 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Antihelix, abnormal | HP:0009738 | T0671 | |
phenodb:0431 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Antitragus, abnormal | HP:0009896 | T0678 | |
phenodb:0432 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Crus | HP:0009895 | ||
phenodb:2975 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Crus > Horizontal | HP:0009897 | T0631 | |
phenodb:0433 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Crus > Prominent | HP:0009899 | a0ee2a626647e6be | |
phenodb:0434 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Crus > Small | HP:0009898 | c268f54e3f240d68 | |
phenodb:0435 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Helix | HP:0011039 | T0628 | |
phenodb:2977 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Helix > Calcified ear cartilage | HP:0005103 | T0646 | |
phenodb:0436 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Helix > Crumpled | HP:0009901 | T0651 | 9f93cc26e0da17b6 |
phenodb:0437 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Helix > Cupped ears | HP:0000378 | T0629 | f80f8a26dad490c9 |
phenodb:2976 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Helix > Hypoplastic ear cartilage | HP:0100720 | ||
phenodb:0441 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Helix > Notched | HP:0009902 | T0657 | |
phenodb:0442 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Helix > Overfolded | HP:0000396 | T0647 | |
phenodb:0443 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Helix > Pits | HP:0008523 | ||
phenodb:0444 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Helix > Simple | HP:0008577 | ||
phenodb:0445 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Helix > Small | HP:0008589 | ||
phenodb:0446 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Helix > Telangiectasia | HP:0009893 | T0627 | |
phenodb:0447 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Helix > Thick | HP:0009894 | T0634 | |
phenodb:0448 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Lobes | HP:0000363 | T0667 | |
phenodb:0449 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Lobes > Absent | HP:0000387 | T0661 | 840bb56a627f1475 |
phenodb:0450 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Lobes > Attached | HP:0009907 | T0662 | 60cabac08fa4d9dd |
phenodb:2978 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Lobes > Cleft | HP:0011265 | T0664 | |
phenodb:0451 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Lobes > Creases | HP:0009908 | T0668 | |
phenodb:0452 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Lobes > Fleshy | HP:0009748 | fbe9aaa78f2f4e2d | |
phenodb:0453 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Lobes > Hypoplastic / Small | HP:0000385 | T0663 | 78a1f63d1b14a563 |
phenodb:2979 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Lobes > Large | HP:0009748 | T0666 | |
phenodb:0454 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Lobes > Pits | |||
phenodb:2980 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Lobes > Uplifted | HP:0009909 | T0670 | |
phenodb:0455 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Tragus | HP:0009912 | T0673 | |
phenodb:2981 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Tragus > Absent | HP:0011268 | T0674 | |
phenodb:0456 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Tragus > Large | HP:0011271 | 4032466fb3837d61 | |
phenodb:0457 | HEAD AND NECK: Ears / Hearing > Structure > External ear > Tragus > Small | HP:0009913 | 8d8e657ae8008656 | |
phenodb:2982 | HEAD AND NECK: Ears / Hearing > Structure > Middle Ear | HP:0000370 | T0682 | |
phenodb:0459 | HEAD AND NECK: Ears / Hearing > Structure > Middle Ear > Auditory canal | HP:0000372 | ||
phenodb:0460 | HEAD AND NECK: Ears / Hearing > Structure > Middle Ear > Auditory canal > Atresia | HP:0011386 | T0681 | |
phenodb:0461 | HEAD AND NECK: Ears / Hearing > Structure > Middle Ear > Auditory canal > Duplication | |||
phenodb:0462 | HEAD AND NECK: Ears / Hearing > Structure > Middle Ear > Auditory canal > Stenosis | HP:0000402 | T0641 | |
phenodb:0465 | HEAD AND NECK: Ears / Hearing > Structure > Middle Ear > Ossicles | HP:0004452 | T0684 | |
phenodb:0467 | HEAD AND NECK: Ears / Hearing > Structure > Middle Ear > Ossicles > Absent | HP:0009910 | ||
phenodb:0466 | HEAD AND NECK: Ears / Hearing > Structure > Middle Ear > Ossicles > Malformed | HP:0004452 | ||
phenodb:0468 | HEAD AND NECK: Ears / Hearing > Structure > Middle Ear > Stapes fixation (ankylosis) | HP:0000381 | T0686 | |
phenodb:0458 | HEAD AND NECK: Ears / Hearing > Structure > Inner ear | HP:0000359 | T0691 | |
phenodb:2983 | HEAD AND NECK: Ears / Hearing > Structure > Inner ear > Anomaly of the semicircular canals | HP:0011380 | T0688 | |
phenodb:0463 | HEAD AND NECK: Ears / Hearing > Structure > Inner ear > Cochlear malformation | HP:0008554 | ||
phenodb:2915 | HEAD AND NECK: Ears / Hearing > Structure > Inner ear > Enlarged vestibular aqueduct | HP:0001387 | ||
phenodb:0464 | HEAD AND NECK: Ears / Hearing > Structure > Inner ear > Mondini malformation | HP:0000376 | T0693 | |
phenodb:0469 | HEAD AND NECK: Ears / Hearing > Structure > Inner ear > Vestibular abnormality | HP:0011376 | T0689 | |
phenodb:0470 | HEAD AND NECK: Ears / Hearing > Function / Hearing | HP:0000364 | T0706 | |
phenodb:3668 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Functional abnormality of the inner ear | HP:0011389 | T0702 | |
phenodb:0471 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Hyperacusis | HP:0010780 | T0704 | |
phenodb:2984 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Tinnitus | HP:0000360 | T0703 | |
phenodb:0472 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Hearing loss | HP:0000365 | T0707 | |
phenodb:0473 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Hearing loss > Type | HP:0000365 | ||
phenodb:2985 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Hearing loss > Type > Central | |||
phenodb:0474 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Hearing loss > Type > Conductive | HP:0000405 | T0722 | |
phenodb:0475 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Hearing loss > Type > Sensorineural | HP:0000407 | T0721 | |
phenodb:0476 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Hearing loss > Type > Mixed conductive, sensorineural | HP:0000410 | T0712 | |
phenodb:0477 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Hearing loss > Type > Unknown | |||
phenodb:0478 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Hearing loss > Timing | |||
phenodb:0479 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Hearing loss > Timing > Acquired | |||
phenodb:0480 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Hearing loss > Timing > Congenital | HP:0000365 | ||
phenodb:0481 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Hearing loss > Timing > Progressive | HP:0001730 | T0717 | |
phenodb:0482 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Hearing loss > Timing > Static | |||
phenodb:0483 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Hearing loss > Timing > Unknown | |||
phenodb:0484 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Hearing loss > Location | |||
phenodb:0485 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Hearing loss > Location > Bilateral | |||
phenodb:0486 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Hearing loss > Location > Unilateral | HP:0009900 | T0719 | |
phenodb:0487 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Hearing loss > Location > Unknown | |||
phenodb:0488 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Hearing loss > Severity | |||
phenodb:0489 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Hearing loss > Severity > Mild | HP:0012712 | T0708 | |
phenodb:0490 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Hearing loss > Severity > Moderate | HP:0012713 | T0709 | |
phenodb:0491 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Hearing loss > Severity > Severe | |||
phenodb:0492 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Hearing loss > Severity > Profound (deaf) | HP:0012715 | T0710 | |
phenodb:0493 | HEAD AND NECK: Ears / Hearing > Function / Hearing > Hearing loss > Severity > Unknown | |||
phenodb:0494 | HEAD AND NECK: Nose | HP:0000366 | T0401 | |
phenodb:0495 | HEAD AND NECK: Nose > Structure | HP:0000366 | ||
phenodb:0496 | HEAD AND NECK: Nose > Structure > General | |||
phenodb:0497 | HEAD AND NECK: Nose > Structure > General > Absent | HP:0009927 | T0424 | c77d436cbcfcdd63 |
phenodb:0498 | HEAD AND NECK: Nose > Structure > General > Bifid | HP:0011803 | T0439 | 7124d8708f2360b3 |
phenodb:0499 | HEAD AND NECK: Nose > Structure > General > Bulbous (aka Bulbous nasal tip and Pear-shaped nose) | HP:0000414 | 042e23a2026636c8 | |
phenodb:0500 | HEAD AND NECK: Nose > Structure > General > Long | HP:0003189 | T0428 | 170bfc5a5c12fecb |
phenodb:0501 | HEAD AND NECK: Nose > Structure > General > Prominent (aka Large nose) | HP:0000448 | T0427 | 2d1e9bde1c9154c4 |
phenodb:0502 | HEAD AND NECK: Nose > Structure > General > Proboscis | HP:0012806 | 771f667b2368ec93 | |
phenodb:0503 | HEAD AND NECK: Nose > Structure > General > Short | HP:0003196 | T0435 | daeb9fb85b0b970f |
phenodb:0504 | HEAD AND NECK: Nose > Structure > General > Wide (aka Broad nose) | HP:0000445 | T0430 | 46d19037adf1a435 |
phenodb:0505 | HEAD AND NECK: Nose > Structure > General > Other feature | |||
phenodb:0506 | HEAD AND NECK: Nose > Structure > Alae nasi | HP:0000429 | T0412 | |
phenodb:0507 | HEAD AND NECK: Nose > Structure > Alae nasi > Cleft (aka Ala nasi, Notched, Ala nasi coloboma) | HP:0003191 | T0526 | 4856efaad5238738 |
phenodb:0508 | HEAD AND NECK: Nose > Structure > Alae nasi > Thick | HP:0009928 | T0450 | 36070ca17ec736f2 |
phenodb:0509 | HEAD AND NECK: Nose > Structure > Alae nasi > Underdeveloped (aka Ala nasi hypoplastic) | HP:0000430 | T0449 | c1129f687f9243b5 |
phenodb:0510 | HEAD AND NECK: Nose > Structure > Alae nasi > Other feature | |||
phenodb:0511 | HEAD AND NECK: Nose > Structure > Columella | HP:0009929 | T0467 | |
phenodb:0512 | HEAD AND NECK: Nose > Structure > Columella > Broad (aka Columella wide) | HP:0010761 | T0468 | 7d4225feb7a8771b |
phenodb:0513 | HEAD AND NECK: Nose > Structure > Columella > Long (aka Columella low, Columella rounded) | HP:0009765 | ||
phenodb:0514 | HEAD AND NECK: Nose > Structure > Columella > High insertion | HP:0012807 | 04895dd7ae88810b | |
phenodb:0515 | HEAD AND NECK: Nose > Structure > Columella > Low insertion | HP:0010763 | T0470 | 49acd433e354541b |
phenodb:2986 | HEAD AND NECK: Nose > Structure > Columella > Low hanging | HP:0009765 | T2901 | |
phenodb:0516 | HEAD AND NECK: Nose > Structure > Columella > Short | HP:0002000 | T0469 | 9bf02f584f83b723 |
phenodb:0517 | HEAD AND NECK: Nose > Structure > Columella > Other feature | |||
phenodb:0518 | HEAD AND NECK: Nose > Structure > Nares | HP:0005288 | ||
phenodb:0519 | HEAD AND NECK: Nose > Structure > Nares > Anteverted (aka Anteverted nostrils, Winged ala nasi, Upturned nasal tip) | HP:0000463 | T0436 | d7284223e790d7aa |
phenodb:2987 | HEAD AND NECK: Nose > Structure > Nares > Asymmetric | HP:0009930 | T0415 | |
phenodb:0520 | HEAD AND NECK: Nose > Structure > Nares > Enlarged | HP:0009931 | T0414 | 39ebb90649f3c38a |
phenodb:0521 | HEAD AND NECK: Nose > Structure > Nares > Narrow (aka Slit-like naris) | HP:0009933 | T0451 | 8b9d29aa3e1824cb |
phenodb:0522 | HEAD AND NECK: Nose > Structure > Nares > Single | HP:0009932 | T0441 | 1e8864b52f21e78d |
phenodb:0523 | HEAD AND NECK: Nose > Structure > Nares > Supernumerary | HP:0009934 | T0438 | b427f756518b51d3 |
phenodb:0524 | HEAD AND NECK: Nose > Structure > Nares > Other feature | |||
phenodb:0525 | HEAD AND NECK: Nose > Structure > Nasal base | HP:0012808 | ||
phenodb:0526 | HEAD AND NECK: Nose > Structure > Nasal base > Narrow | HP:0012809 | fc8449da66ac70e5 | |
phenodb:0527 | HEAD AND NECK: Nose > Structure > Nasal base > Wide | HP:0012810 | 4a8c3cd977c27473 | |
phenodb:0528 | HEAD AND NECK: Nose > Structure > Nasal base > Other feature | |||
phenodb:0529 | HEAD AND NECK: Nose > Structure > Nasal bridge | HP:0000422 | T0402 | |
phenodb:0530 | HEAD AND NECK: Nose > Structure > Nasal bridge > Depressed (aka Flat, Low, Recessed, Retruded) | HP:0005280 | T0406 | 000fb29123c16757 |
phenodb:0531 | HEAD AND NECK: Nose > Structure > Nasal bridge > Narrow (aka Nasal bridge thin) | HP:0000446 | T0433 | 87f7fd4185cf006d |
phenodb:0532 | HEAD AND NECK: Nose > Structure > Nasal bridge > Prominent (aka Nasal bridge, high) | HP:0000426 | T0405 | a7571049e570041c |
phenodb:0533 | HEAD AND NECK: Nose > Structure > Nasal bridge > Wide (aka Nasal bridge, broad) | HP:0000431 | T0431 | e29866db35162165 |
phenodb:0534 | HEAD AND NECK: Nose > Structure > Nasal bridge > Other feature | |||
phenodb:0535 | HEAD AND NECK: Nose > Structure > Nasal cartilage, absent | HP:0005273 | T0445 | 73e4e8bb2eec316d |
phenodb:0536 | HEAD AND NECK: Nose > Structure > Nasal ridge | HP:0011119 | T0407 | |
phenodb:0537 | HEAD AND NECK: Nose > Structure > Nasal ridge > Concave (aka Saddle nose and Ski jump nose) | HP:0011120 | T0409 | d1fbc39bb2a7200c |
phenodb:0538 | HEAD AND NECK: Nose > Structure > Nasal ridge > Convex (aka Beaked nose and Hooked nose) | HP:0000444 | T0444 | 828a352227deae4b |
phenodb:0539 | HEAD AND NECK: Nose > Structure > Nasal ridge > Depressed (aka Flat nose) | HP:0000457 | T0437 | d63325b1b95d9849 |
phenodb:0540 | HEAD AND NECK: Nose > Structure > Nasal ridge > Narrow (aka Pinched nose) | HP:0000418 | T0408 | 506b9fe34efcb05f |
phenodb:0541 | HEAD AND NECK: Nose > Structure > Nasal ridge > Paranasal fullness (aka Laterally built up nose) | HP:0012812 | edd8027f8704eb10 | |
phenodb:0542 | HEAD AND NECK: Nose > Structure > Nasal ridge > Wide (aka Broad nasal ridge) | HP:0012811 | e4f7eb8e1c23a1c8 | |
phenodb:0543 | HEAD AND NECK: Nose > Structure > Nasal ridge > Other feature | |||
phenodb:0544 | HEAD AND NECK: Nose > Structure > Nasal tip | HP:0000436 | T0416 | |
phenodb:0545 | HEAD AND NECK: Nose > Structure > Nasal tip > Bifid (aka Bifid nasal tip) | HP:0000456 | T0440 | 55d70204f2c9fd1c |
phenodb:0546 | HEAD AND NECK: Nose > Structure > Nasal tip > Broad (aka Bulbous nasal tip) | HP:0000414 | T0429 | 5b055d842e77449b |
phenodb:0547 | HEAD AND NECK: Nose > Structure > Nasal tip > Depressed (aka Retruded or Recessed nasal tip) | HP:0000437 | T0452 | ee92e98f413cf56f |
phenodb:0548 | HEAD AND NECK: Nose > Structure > Nasal tip > Deviated | HP:0011831 | T0419 | c43a1d5ac6da32f0 |
phenodb:0549 | HEAD AND NECK: Nose > Structure > Nasal tip > Narrow (aka Pinched nasal tip) | HP:0011832 | T0418 | a9769c3dacf3fc83 |
phenodb:0550 | HEAD AND NECK: Nose > Structure > Nasal tip > Overhanging | HP:0011833 | T2900 | 44f864fd10dfe496 |
phenodb:0551 | HEAD AND NECK: Nose > Structure > Nasal tip > Other feature | |||
phenodb:2988 | HEAD AND NECK: Nose > Structure > Nasal septum | HP:0000419 | T0420 | |
phenodb:2989 | HEAD AND NECK: Nose > Structure > Nasal septum > Deviated | HP:0004411 | T0456 | |
phenodb:2990 | HEAD AND NECK: Nose > Structure > Nasal septum > Polyp | HP:0100582 | T0459 | |
phenodb:3615 | HEAD AND NECK: Nose > Structure > Nasal septum > Other feature | |||
phenodb:0552 | HEAD AND NECK: Nose > Function | HP:0004408 | T0463 | |
phenodb:0553 | HEAD AND NECK: Nose > Function > Anosmia | HP:0000458 | ||
phenodb:0554 | HEAD AND NECK: Nose > Function > Epistaxis | HP:0000421 | T2605 | |
phenodb:0555 | HEAD AND NECK: Nose > Function > Rhinitis | HP:0012384 | T0462 | |
phenodb:0556 | HEAD AND NECK: Nose > Function > Other feature | |||
phenodb:0557 | HEAD AND NECK: Oral region | |||
phenodb:0558 | HEAD AND NECK: Oral region > Lips | HP:0000159 | T0489 | |
phenodb:0559 | HEAD AND NECK: Oral region > Lips > Cleft | HP:0000204 | T0522 | |
phenodb:2991 | HEAD AND NECK: Oral region > Lips > Cleft > Bilateral | HP:0100336 | T0528 | |
phenodb:0560 | HEAD AND NECK: Oral region > Lips > Cleft > Lateral | HP:0100335 | T0527 | |
phenodb:0561 | HEAD AND NECK: Oral region > Lips > Cleft > Midline | HP:0000161 | T0523 | |
phenodb:0564 | HEAD AND NECK: Oral region > Lips > Commissural pit(s) (pit at the corner of the lips - NOT the same as lip pits) | HP:0002710 | 039dd7f4bd054dc6 | |
phenodb:0567 | HEAD AND NECK: Oral region > Lips > Cupid's bow | |||
phenodb:0568 | HEAD AND NECK: Oral region > Lips > Cupid's bow > Absent | HP:0010800 | T0486 | 72c0a8d95e9ece54 |
phenodb:0569 | HEAD AND NECK: Oral region > Lips > Cupid's bow > Exaggerated (aka Cupid's bow / Accentuated cupid's bow / Tented upper lip) | HP:0002263 | T0506 | abb6065ac4f2f9d6 |
phenodb:0570 | HEAD AND NECK: Oral region > Lips > Cupid's bow > Other feature | |||
phenodb:0571 | HEAD AND NECK: Oral region > Lips > Freckle(s) (aka Lip lentigo / Lip lentigenes) | HP:0010798 | T0509 | 8280aa96e24e69de |
phenodb:0572 | HEAD AND NECK: Oral region > Lips > Lower lip | HP:0000178 | T0511 | |
phenodb:2992 | HEAD AND NECK: Oral region > Lips > Lower lip > Cleft | HP:0010281 | T0513 | |
phenodb:0573 | HEAD AND NECK: Oral region > Lips > Lower lip > Everted (aka Vermillion, lower lip everted / drooping lower lip) | HP:0000232 | T0512 | 7a571bf428560137 |
phenodb:0574 | HEAD AND NECK: Oral region > Lips > Lower lip > Thick (aka Vermillion, lower lip thick / full lower lip / thick lower lip / prominent lower lip) | HP:0000179 | T0497 | ec0d200ae22ef2dc |
phenodb:0575 | HEAD AND NECK: Oral region > Lips > Lower lip > Thin (aka Vermillion, lower lip thin / narrow lower lip) | HP:0010282 | T0500 | 83080988670111f0 |
phenodb:0576 | HEAD AND NECK: Oral region > Lips > Lower lip > Other feature | |||
phenodb:0577 | HEAD AND NECK: Oral region > Lips > Nasolabial fold | |||
phenodb:0578 | HEAD AND NECK: Oral region > Lips > Nasolabial fold > Prominent (aka Deep nasolabial fold or crease / Prominent nasolabial crease) | HP:0005272 | T0091 | 0f154316243118b9 |
phenodb:0579 | HEAD AND NECK: Oral region > Lips > Nasolabial fold > Underdeveloped (aka Smooth nasolabial fold or crease / Hypoplastic nasolabial fold or crease) | HP:0010801 | T0092 | 9270f3697f4bc7b7 |
phenodb:0580 | HEAD AND NECK: Oral region > Lips > Nasolabial fold > Other feature | |||
phenodb:0581 | HEAD AND NECK: Oral region > Lips > Philtrum | HP:0000288 | ||
phenodb:0582 | HEAD AND NECK: Oral region > Lips > Philtrum > Broad (aka Wide philtrum) | HP:0000289 | T0487 | 1fdb03ff8bb336d0 |
phenodb:0583 | HEAD AND NECK: Oral region > Lips > Philtrum > Deep (aka Prominent philtrum / Depressed philtrum) | HP:0002002 | T0484 | 3c771454d4293f5e |
phenodb:0584 | HEAD AND NECK: Oral region > Lips > Philtrum > Long | HP:0000343 | T0482 | e1d74175c310388d |
phenodb:0585 | HEAD AND NECK: Oral region > Lips > Philtrum > Midline raphe | HP:0011826 | 10c606d126a4db12 | |
phenodb:0586 | HEAD AND NECK: Oral region > Lips > Philtrum > Midline sinus | HP:0011828 | T0481 | 6c2fb154a038ab64 |
phenodb:0587 | HEAD AND NECK: Oral region > Lips > Philtrum > Narrow | HP:0011829 | T0478 | 14084d321e471f2a |
phenodb:0588 | HEAD AND NECK: Oral region > Lips > Philtrum > Ridges, malaligned | HP:0011827 | T0480 | a5201703ffd4c09f |
phenodb:0589 | HEAD AND NECK: Oral region > Lips > Philtrum > Short | HP:0000322 | T0483 | 7d7813d2713bd4d2 |
phenodb:0590 | HEAD AND NECK: Oral region > Lips > Philtrum > Smooth (aka Flat philtrum / Indistinct philtrum / Simple philtrum) | HP:0000319 | T0485 | 3abca500a8f1872a |
phenodb:0591 | HEAD AND NECK: Oral region > Lips > Philtrum > Tented | HP:0011825 | T0479 | 276be153ab66593d |
phenodb:0592 | HEAD AND NECK: Oral region > Lips > Philtrum > Other feature | |||
phenodb:0593 | HEAD AND NECK: Oral region > Lips > Pit(s) (aka Lip fistula / Lip fistulae) | HP:0100267 | T0507 | 54f2dee42a1f9ef7 |
phenodb:2993 | HEAD AND NECK: Oral region > Lips > Protruding | |||
phenodb:2994 | HEAD AND NECK: Oral region > Lips > Thick | HP:0012471 | ||
phenodb:2995 | HEAD AND NECK: Oral region > Lips > Thin | HP:0000233 | T0499 | |
phenodb:0596 | HEAD AND NECK: Oral region > Lips > Upper lip | HP:0000177 | T0515 | |
phenodb:0597 | HEAD AND NECK: Oral region > Lips > Upper lip > Everted (aka Vermillion upper lip, everted) | HP:0010803 | T0516 | 97d86f6834b60d20 |
phenodb:0598 | HEAD AND NECK: Oral region > Lips > Upper lip > Tented (aka Vermillion upper lip, tented and tented mouth) | HP:0010804 | T0518 | d7fcae8f3276b13a |
phenodb:0599 | HEAD AND NECK: Oral region > Lips > Upper lip > Thick (aka Vermillion upper lip, thick / coarse upper lip / full upper lip / prominent upper lip) | HP:0000215 | T0496 | e6ac74e7bedf0e51 |
phenodb:0600 | HEAD AND NECK: Oral region > Lips > Upper lip > Thin (aka Vermillion upper lip, thin / thin vermillion border) | HP:0000219 | a5293d97f7bfc31c | |
phenodb:0601 | HEAD AND NECK: Oral region > Lips > Upper lip > U-shaped | HP:0010806 | T0517 | 34e1c568648c7eea |
phenodb:0602 | HEAD AND NECK: Oral region > Lips > Upper lip > Other feature | |||
phenodb:0603 | HEAD AND NECK: Oral region > Mouth / Oropharynx | HP:0000153 | T0488 | |
phenodb:0604 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Alveolar ridge overgrowth (aka Hypertrophic alveolar ridge / Alveolar ridge hypertrophy) | HP:0009085 | T0550 | 6ef36fa1dadd90f9 |
phenodb:2996 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Anomaly of the oral cavity | HP:0000163 | ||
phenodb:3013 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Anomaly of the oral mucosa | HP:0011830 | T0546 | |
phenodb:3669 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Anomaly of the oral mucosa > Mucosal telangiectasia | HP:0100579 | T1311 | |
phenodb:0605 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Ankyloglossia (aka Tongue-tie / Tongue tied) | HP:0010296 | T0544 | 920b3a970339ac8a |
phenodb:2997 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Chelitis | HP:0100825 | T0519 | |
phenodb:0606 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Drooling | HP:0002307 | ||
phenodb:0607 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Fibrous syngnathia (aka Fused alveloar ridges) | HP:0009754 | T0160 | 845ab90722d28487 |
phenodb:0608 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Gingiva | HP:0000168 | T0531 | |
phenodb:2998 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Gingiva > Cleft alveolar ridge | HP:0010289 | T0525 | |
phenodb:2999 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Gingiva > Gingival hemorrhage | HP:0000225 | T2606 | |
phenodb:0610 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Gingiva > Gingivitis | HP:0000230 | T0557 | |
phenodb:0609 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Gingiva > Overgrowth (aka Gingival hyperplasia / Gingival hypertrophy) | HP:0000212 | T0552 | b4c5a697fbc5e871 |
phenodb:0611 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Gingiva > Other feature | |||
phenodb:0612 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Glossoptosis | HP:0000162 | T0540 | ddc1a2c7e23644e8 |
phenodb:3000 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Halitosis | HP:0100812 | T1489 | |
phenodb:0613 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Hyperpigmentation, intra-oral | HP:0010284 | T0556 | 3ba03107669230ee |
phenodb:3001 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Leukoplakia | HP:0002745 | T1264 | |
phenodb:0614 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Mouth, shape | HP:0011338 | ||
phenodb:3002 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Mouth, shape > Asymmetric | HP:0009941 | T0492 | |
phenodb:0615 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Mouth, shape > Downturned corners (aka Carp mouth / Fish mouth) | HP:0002714 | T0503 | 701f27bab4ac3f92 |
phenodb:0616 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Mouth, shape > Narrow (aka Microstomia and small mouth / Small oral aperture) | HP:0000160 | T0494 | dbaf4cd806daeacb |
phenodb:3003 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Mouth, shape > Open | HP:0000194 | T0505 | |
phenodb:0617 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Mouth, shape > Upturned corners | HP:0010805 | T0490 | ec8693737e10d7ab |
phenodb:0618 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Mouth, shape > Wide (aka Macrostomia / Large mouth / Large oral aperture) | HP:0000154 | T0493 | a6a2d57a281ead72 |
phenodb:0619 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Mouth, shape > Other feature | |||
phenodb:0620 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Open bite (aka Malocclusion) | HP:0010807 | T0162 | 10b2b6e5a7551847 |
phenodb:0621 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Oral frenula, accessory (aka Oral frenula / Supernumerary oral frenula) | HP:0000191 | T0553 | 57fbd034f7a61e60 |
phenodb:0622 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Oral synechia | HP:0010285 | T0549 | 9d6b7c2eb57b8e7c |
phenodb:1044 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Oropharyngeal dysphagia | HP:0200136 | ||
phenodb:0623 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Palate | HP:0000174 | T0558 | |
phenodb:0624 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Palate > Cleft | HP:0000175 | T0574 | |
phenodb:3004 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Palate > Cleft > Bilateral | HP:0100337 | T0575 | |
phenodb:0625 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Palate > Cleft > Lateral | HP:0100337 | ||
phenodb:0626 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Palate > Cleft > Midline | HP:0009099 | ||
phenodb:0629 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Palate > Cleft > Other feature | |||
phenodb:3005 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Palate > Fistula | HP:0010294 | T0560 | |
phenodb:0630 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Palate > Hard, short (aka Short palate / Hypoplastic palate) | HP:0010290 | T0563 | db6ea87e74a51c8a |
phenodb:0631 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Palate > High (aka High arched palate) | HP:0000218 | T0562 | 51755789482fe3a8 |
phenodb:0632 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Palate > Narrow | HP:0000189 | T0561 | 70a0a128965515c4 |
phenodb:0633 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Palate > Submucous cleft | HP:0011819 | T0573 | 30b9e9da9758d9d7 |
phenodb:3006 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Palate > Torus palatini | HP:0100789 | T0564 | |
phenodb:0634 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Palatine ridges, prominent | HP:0010291 | T0559 | de4e86bf37f3bbf1 |
phenodb:0635 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Periodontitis | HP:0000704 | T0616 | |
phenodb:0636 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Salivary gland abnormalities | HP:0010286 | T1419 | |
phenodb:3009 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Salivary gland abnormalities > Excessive salivation | HP:0003781 | T1487 | |
phenodb:3010 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Salivary gland abnormalities > Reduced salivation | HP:0000217 | T1488 | |
phenodb:0637 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Salivary gland abnormalities > Specify | |||
phenodb:3007 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Soft palate anomaly | HP:0100736 | ||
phenodb:3008 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Stomatitis | HP:0010280 | T0547 | |
phenodb:0638 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Tongue | HP:0000157 | T0532 | |
phenodb:0639 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Tongue > Bifid (aka Split tongue / Snake tongue) | HP:0010297 | T0542 | 1af98064c7272d0a |
phenodb:0640 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Tongue > Furrowed (aka Prominent or deep tongue grooves / Geographic tongue and scrotal tongue) | HP:0000221 | T0543 | 97b601adeb79955a |
phenodb:3011 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Tongue > Glossitis | HP:0000206 | T0545 | |
phenodb:3012 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Tongue > Glossopalatal ankylosis | |||
phenodb:0641 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Tongue > Hamartoma | HP:0000180 | T0537 | |
phenodb:0642 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Tongue > Large (aka Macroglossia / Hyperplastic tongue and hypertrophic tongue) | HP:0000158 | T0535 | 9638e4ba815e5908 |
phenodb:0643 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Tongue > Lobulated (aka Lobed or bilobed or trilobed tongue) | HP:0000180 | T0538 | f273ff393ebab6af |
phenodb:0644 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Tongue > Protruding | HP:0010808 | T0534 | d412486c2b3e365a |
phenodb:0645 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Tongue > Small (aka Microglossia / Hypoglossia / Hypoplastic tongue / Aglossia / Rudimentary tongue) | HP:0000171 | T0536 | e801e8c7a523ec7f |
phenodb:0646 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Tongue > Smooth | HP:0010298 | T0533 | 6742bac323d3cfe9 |
phenodb:0647 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Tongue > Other feature | |||
phenodb:0648 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Trismus | HP:0000211 | T2389 | |
phenodb:0649 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Ulcers, oral | HP:0000155 | T0548 | |
phenodb:0650 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Uvula | HP:0000172 | ||
phenodb:0651 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Uvula > Absent | HP:0010292 | T0568 | 8b9d550b8b96c39e |
phenodb:0652 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Uvula > Bifid (aka Cleft uvula) | HP:0000193 | T0571 | 89bbddff1c94bf45 |
phenodb:0653 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Uvula > Broad (aka Thick uvula / Wide uvula) | HP:0010809 | T0567 | 7a5d2cf40398f848 |
phenodb:0654 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Uvula > Long | HP:0010810 | T0566 | 826a4e437174b450 |
phenodb:0655 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Uvula > Narrow | HP:0010811 | T0570 | 13035e06c3c1d73a |
phenodb:0656 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Uvula > Short | HP:0010812 | T0569 | 3a856a6cf478f138 |
phenodb:0657 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Uvula > Other feature | |||
phenodb:0658 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Xerostomia (aka Dry mouth) | HP:0000217 | ||
phenodb:2873 | HEAD AND NECK: Oral region > Mouth / Oropharynx > Other feature | |||
phenodb:0659 | HEAD AND NECK: Teeth | HP:0000164 | T0577 | |
phenodb:0660 | HEAD AND NECK: Teeth > Eruption / Loss | HP:0006292 | ||
phenodb:0661 | HEAD AND NECK: Teeth > Eruption / Loss > Advanced | HP:0006288 | T0608 | 054a0d72d8bcc41d |
phenodb:0662 | HEAD AND NECK: Teeth > Eruption / Loss > Delayed | HP:0000684 | T0612 | 78d33d68e0aba09c |
phenodb:0663 | HEAD AND NECK: Teeth > Eruption / Loss > Neonatal tooth (aka Natal teeth) | HP:0000695 | T0609 | c1c1c4d708172d57 |
phenodb:3014 | HEAD AND NECK: Teeth > Eruption / Loss > Premature loss of primary teeth | HP:0006323 | T0611 | |
phenodb:0664 | HEAD AND NECK: Teeth > Eruption / Loss > Premature loss of secondary teeth | HP:0006357 | T0579 | 77725e7564f6808c |
phenodb:0665 | HEAD AND NECK: Teeth > Eruption / Loss > Other feature | |||
phenodb:0666 | HEAD AND NECK: Teeth > Position | |||
phenodb:0667 | HEAD AND NECK: Teeth > Position > Dental crowding | HP:0000678 | T0598 | 997c7a12a3ac4f88 |
phenodb:0668 | HEAD AND NECK: Teeth > Position > Diastema (wide space between two adjacent teeth) | HP:0000699 | 741294084e243d0a | |
phenodb:0669 | HEAD AND NECK: Teeth > Position > Labial teeth | |||
phenodb:0670 | HEAD AND NECK: Teeth > Position > Widely spaced teeth | HP:0000687 | T2902 | fb854d4a5b04957d |
phenodb:0671 | HEAD AND NECK: Teeth > Position > Other feature | |||
phenodb:0672 | HEAD AND NECK: Teeth > Structure / Size / Number | HP:0006483 | ||
phenodb:3026 | HEAD AND NECK: Teeth > Structure / Size / Number > Abnormal resorption of teeth | |||
phenodb:3025 | HEAD AND NECK: Teeth > Structure / Size / Number > Abnormality of dental color | HP:0011073 | T0606 | |
phenodb:3023 | HEAD AND NECK: Teeth > Structure / Size / Number > Abnormality of dental enamel | HP:0000682 | T0601 | |
phenodb:3024 | HEAD AND NECK: Teeth > Structure / Size / Number > Abnormality of the dentin | HP:0010299 | T0603 | |
phenodb:3017 | HEAD AND NECK: Teeth > Structure / Size / Number > Abnormally shaped teeth | HP:0006482 | T0583 | |
phenodb:3020 | HEAD AND NECK: Teeth > Structure / Size / Number > Absent canines | HP:0012738 | T0596 | |
phenodb:3018 | HEAD AND NECK: Teeth > Structure / Size / Number > Absent incisors | HP:0006485 | ||
phenodb:3019 | HEAD AND NECK: Teeth > Structure / Size / Number > Absent molars | HP:0011054 | T0595 | |
phenodb:0673 | HEAD AND NECK: Teeth > Structure / Size / Number > Amelogenesis imperfecta | HP:0000705 | T0602 | |
phenodb:0674 | HEAD AND NECK: Teeth > Structure / Size / Number > Anodontia | HP:0000674 | T0590 | 74e893c894584eb8 |
phenodb:0675 | HEAD AND NECK: Teeth > Structure / Size / Number > Caries | HP:0000670 | T0607 | |
phenodb:0676 | HEAD AND NECK: Teeth > Structure / Size / Number > Central incisor, single maxillary | HP:0006315 | T0593 | e271e640309491ed |
phenodb:0677 | HEAD AND NECK: Teeth > Structure / Size / Number > Conical teeth (aka Peg-shaped teeth) | HP:0000698 | T0584 | |
phenodb:0678 | HEAD AND NECK: Teeth > Structure / Size / Number > Dentinogenesis imperfecta | HP:0000703 | T0604 | |
phenodb:3022 | HEAD AND NECK: Teeth > Structure / Size / Number > Diastema (wide space between two adjacent teeth) | HP:0000699 | ||
phenodb:0679 | HEAD AND NECK: Teeth > Structure / Size / Number > Fused teeth (aka Double tooth / Dental fusion) | HP:0011090 | T0580 | f3a0d2fb178105d7 |
phenodb:3021 | HEAD AND NECK: Teeth > Structure / Size / Number > Impacted tooth | HP:0011079 | T0597 | |
phenodb:0680 | HEAD AND NECK: Teeth > Structure / Size / Number > Macrodontia (aka Large teeth and wide teeth / Hyperplastic teeth) | HP:0001572 | T0587 | b8258ffc2ff9d364 |
phenodb:0681 | HEAD AND NECK: Teeth > Structure / Size / Number > Microdontia (aka Small teeth / Narrow teeth / Hypoplastic teeth) | HP:0000691 | T0586 | 384c1789373a700e |
phenodb:0682 | HEAD AND NECK: Teeth > Structure / Size / Number > Odontogenic keratocysts | HP:0010603 | ||
phenodb:0684 | HEAD AND NECK: Teeth > Structure / Size / Number > Ridged teeth | |||
phenodb:0683 | HEAD AND NECK: Teeth > Structure / Size / Number > Selected tooth agenesis | HP:0006349 | 74e893c894584eb8 | |
phenodb:3016 | HEAD AND NECK: Teeth > Structure / Size / Number > Short dental roots | HP:0006336 | T0582 | |
phenodb:0685 | HEAD AND NECK: Teeth > Structure / Size / Number > Supernumerary tooth (aka Supernumerary teeth / Extra teeth) | HP:0011069 | T0588 | 60888cccac8e54b6 |
phenodb:3015 | HEAD AND NECK: Teeth > Structure / Size / Number > Talon cusp | HP:0011087 | T0581 | |
phenodb:0686 | HEAD AND NECK: Teeth > Structure / Size / Number > Taurodontism | HP:0000679 | T0585 | |
phenodb:0687 | HEAD AND NECK: Teeth > Structure / Size / Number > Other feature | |||
phenodb:0688 | HEAD AND NECK: Neck | HP:0000464 | T0727 | |
phenodb:3027 | HEAD AND NECK: Neck > Anomaly of the branchial arch | HP:0009794 | T0695 | |
phenodb:3028 | HEAD AND NECK: Neck > Branchial cleft fistula | HP:0009795 | T0736 | |
phenodb:0689 | HEAD AND NECK: Neck > Branchial clefts, cyst | HP:0009796 | T0735 | |
phenodb:0690 | HEAD AND NECK: Neck > Broad | HP:0000475 | T0730 | 1f45b748bb5aa8fe |
phenodb:0691 | HEAD AND NECK: Neck > Cystic hygroma | HP:0000476 | ||
phenodb:0692 | HEAD AND NECK: Neck > Goiter | HP:0000853 | T2055 | |
phenodb:0693 | HEAD AND NECK: Neck > Long | HP:0000472 | T0729 | 7c963baf8e0fd48f |
phenodb:0694 | HEAD AND NECK: Neck > Nuchal skin, redundant | HP:0005989 | T0733 | 02288646dd433c21 |
phenodb:0695 | HEAD AND NECK: Neck > Short | HP:0000470 | T0731 | c75e63fd749ec7a8 |
phenodb:0696 | HEAD AND NECK: Neck > Thyroglossal duct cyst | HP:0010518 | T0737 | |
phenodb:0697 | HEAD AND NECK: Neck > Torticollis | HP:0000473 | ||
phenodb:3029 | HEAD AND NECK: Neck > Torticollis, congenital | HP:0005988 | T0738 | |
phenodb:0698 | HEAD AND NECK: Neck > Webbed | HP:0000465 | T0732 | 1236af621234b150 |
phenodb:0699 | HEAD AND NECK: Neck > Other feature | |||
phenodb:0700 | VOICE: | HP:0001608 | T1671 | |
phenodb:3030 | VOICE: Abnormal cry | |||
phenodb:0701 | VOICE: Abnormally low-pitched voice | HP:0010300 | T1678 | |
phenodb:0702 | VOICE: Cat-like cry | HP:0200046 | ||
phenodb:3031 | VOICE: High-pitch cry | |||
phenodb:0703 | VOICE: High-pitched voice | HP:0001620 | T1677 | |
phenodb:0704 | VOICE: Hoarse voice | HP:0001609 | T1675 | |
phenodb:0705 | VOICE: Loss of voice | HP:0001686 | ||
phenodb:0706 | VOICE: Nasal voice / Hypernasal voice / Nasal speech | HP:0001611 | T1672 | |
phenodb:0707 | VOICE: Soft voice | HP:0001621 | T1680 | |
phenodb:0708 | VOICE: Weak cry | HP:0001612 | T1679 | |
phenodb:0709 | VOICE: Other feature | |||
phenodb:0710 | CHEST / THORAX: | HP:0000765 | T0740 | |
phenodb:0711 | CHEST / THORAX: External features | |||
phenodb:0712 | CHEST / THORAX: External features > Chest shape | HP:0000765 | ||
phenodb:0713 | CHEST / THORAX: External features > Chest shape > Asymmetric | HP:0001555 | T0775 | |
phenodb:0714 | CHEST / THORAX: External features > Chest shape > Barrel-shaped | HP:0001552 | T0745 | |
phenodb:0715 | CHEST / THORAX: External features > Chest shape > Bell-shaped | HP:0001591 | T0776 | |
phenodb:0716 | CHEST / THORAX: External features > Chest shape > Broad | HP:0000914 | ||
phenodb:0717 | CHEST / THORAX: External features > Chest shape > Funnel | |||
phenodb:0718 | CHEST / THORAX: External features > Chest shape > Narrow | HP:0000774 | T0770 | |
phenodb:0719 | CHEST / THORAX: External features > Chest shape > Small | HP:0005257 | ||
phenodb:0720 | CHEST / THORAX: External features > Chest shape > Other feature | |||
phenodb:0721 | CHEST / THORAX: External features > Shoulders | HP:0003043 | ||
phenodb:0722 | CHEST / THORAX: External features > Shoulders > Narrow | |||
phenodb:0723 | CHEST / THORAX: External features > Shoulders > Sloping | HP:0200021 | T0767 | |
phenodb:3032 | CHEST / THORAX: External features > Shoulders > Synostosis | HP:0006595 | ||
phenodb:0724 | CHEST / THORAX: External features > Shoulders > Other feature | |||
phenodb:0725 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae | |||
phenodb:0726 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Ribs | HP:0000772 | T0746 | |
phenodb:0727 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Ribs > Absent | HP:0000921 | T0748 | |
phenodb:0728 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Ribs > Anomalies | HP:0000772 | ||
phenodb:0729 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Ribs > Beaded | HP:0000923 | ||
phenodb:0730 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Ribs > Bifid | HP:0000892 | ||
phenodb:0731 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Ribs > Broad | HP:0000885 | ||
phenodb:0732 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Ribs > Cervical | HP:0000891 | T0755 | |
phenodb:0733 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Ribs > Cupped | HP:0000887 | ||
phenodb:0734 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Ribs > 11 pairs | HP:0000878 | T0749 | |
phenodb:0735 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Ribs > Exostoses | HP:0100777 | ||
phenodb:0736 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Ribs > Extra / Supernumerary | HP:0005815 | T0751 | |
phenodb:3033 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Ribs > Flared | HP:0000904 | T0758 | |
phenodb:0737 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Ribs > Fused | HP:0000902 | T0752 | |
phenodb:0738 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Ribs > Hypoplastic | HP:0000773 | ||
phenodb:0739 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Ribs > Ribbon-like | HP:0010561 | ||
phenodb:0740 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Ribs > Rosary | HP:0010561 | ||
phenodb:0741 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Ribs > Short | HP:0000773 | T0759 | |
phenodb:0742 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Ribs > Thick | HP:0000900 | T0753 | |
phenodb:0743 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Ribs > Thin | HP:0000883 | T0754 | |
phenodb:0744 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Ribs > Other feature | |||
phenodb:0745 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Sternum | HP:0000766 | T0790 | |
phenodb:3034 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Sternum > Bifid sternum | HP:0010309 | T0793 | |
phenodb:0746 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Sternum > Costochondral junction, wide / enlarged | HP:0000920 | ||
phenodb:0747 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Sternum > Pectus carinatum | HP:0000768 | T0795 | |
phenodb:0748 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Sternum > Pectus excavatum | HP:0000767 | T0796 | |
phenodb:0749 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Sternum > Prominent sternum | HP:0000884 | ||
phenodb:0750 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Sternum > Sternum, lack of ossification | HP:0006628 | T0794 | |
phenodb:0751 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Sternum > Sternum, short | HP:0000879 | T0791 | |
phenodb:0752 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Sternum > Other feature | |||
phenodb:0753 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Clavicles | HP:0000889 | T0760 | |
phenodb:3035 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Clavicles > Absent | HP:0006660 | T0762 | |
phenodb:3036 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Clavicles > Bipartite | HP:0006585 | T0766 | |
phenodb:3037 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Clavicles > Bowed | |||
phenodb:0754 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Clavicles > Hooked | HP:0000895 | T0763 | |
phenodb:0755 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Clavicles > Hypoplastic | HP:0000894 | ||
phenodb:0756 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Clavicles > Long | HP:0000890 | ||
phenodb:0757 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Clavicles > Short | HP:0000894 | T0761 | |
phenodb:0758 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Clavicles > Other feature | |||
phenodb:0759 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Scapulae | HP:0000782 | ||
phenodb:3038 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Scapulae > Absent | HP:0010317 | T0962 | |
phenodb:0760 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Scapulae > Anomaly | HP:0000782 | T0957 | |
phenodb:0761 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Scapulae > Exostoses | HP:0100777 | ||
phenodb:0762 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Scapulae > Sclerotic | HP:0001474 | ||
phenodb:0763 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Scapulae > Small / Short / Hypoplastic | HP:0000882 | T0958 | |
phenodb:3039 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Scapulae > Sprengel deformity | HP:0000912 | T0959 | |
phenodb:0764 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Scapulae > Winged | HP:0003691 | T0960 | |
phenodb:0765 | CHEST / THORAX: Ribs, sternum, clavicles, and scapulae > Scapulae > Other feature | |||
phenodb:0766 | CHEST / THORAX: Breasts | HP:0000769 | T0743 | |
phenodb:0767 | CHEST / THORAX: Breasts > Breast, general | HP:0000769 | ||
phenodb:3040 | CHEST / THORAX: Breasts > Breast, general > Absent breast | HP:0100783 | T0786 | |
phenodb:0768 | CHEST / THORAX: Breasts > Breast, general > Asymmetry | HP:0010312 | T0742 | |
phenodb:0769 | CHEST / THORAX: Breasts > Breast, general > Gynecomastia | HP:0000771 | T0788 | |
phenodb:0770 | CHEST / THORAX: Breasts > Breast, general > Hypertrophy | HP:0010313 | ||
phenodb:0771 | CHEST / THORAX: Breasts > Breast, general > Hypoplasia | HP:0003187 | T2903 | |
phenodb:0772 | CHEST / THORAX: Breasts > Breast, general > Hypoplasia > Unilateral | HP:0012813 | ||
phenodb:0773 | CHEST / THORAX: Breasts > Breast, general > Hypoplasia > Bilateral | HP:0012814 | ||
phenodb:2874 | CHEST / THORAX: Breasts > Breast, general > Other feature | |||
phenodb:0774 | CHEST / THORAX: Breasts > Nipples | HP:0004404 | T0778 | |
phenodb:3041 | CHEST / THORAX: Breasts > Nipples > Absent nipples | HP:0002561 | T0783 | |
phenodb:0775 | CHEST / THORAX: Breasts > Nipples > Hypoplastic nipples | HP:0002557 | T0782 | |
phenodb:0776 | CHEST / THORAX: Breasts > Nipples > Hypoplastic areolae | HP:0100853 | T0784 | |
phenodb:0777 | CHEST / THORAX: Breasts > Nipples > Inverted | HP:0003186 | ||
phenodb:0778 | CHEST / THORAX: Breasts > Nipples > Low-set nipples | HP:0002562 | T0780 | |
phenodb:0779 | CHEST / THORAX: Breasts > Nipples > Prominent nipples | HP:0004405 | ||
phenodb:0780 | CHEST / THORAX: Breasts > Nipples > Supernumerary | HP:0002558 | T0781 | |
phenodb:0781 | CHEST / THORAX: Breasts > Nipples > Widely spaced | HP:0006610 | T0779 | |
phenodb:0782 | CHEST / THORAX: Breasts > Nipples > Other feature | |||
phenodb:3042 | CHEST / THORAX: Thymus | HP:0000777 | ||
phenodb:3043 | CHEST / THORAX: Thymus > Absent | HP:0005359 | T1845 | |
phenodb:3044 | CHEST / THORAX: Thymus > Hyperplastic | HP:0010516 | T1846 | |
phenodb:3045 | CHEST / THORAX: Pectoralis muscles | HP:0011957 | ||
phenodb:3046 | CHEST / THORAX: Pectoralis muscles > Absent | HP:0012037 | ||
phenodb:3047 | CHEST / THORAX: Pectoralis muscles > Hypoplastic | HP:0008998 | T2904 | |
phenodb:0783 | CHEST / THORAX: Diaphragm | HP:0000775 | T1571 | |
phenodb:0784 | CHEST / THORAX: Diaphragm > Agenesis | HP:0008986 | ||
phenodb:0785 | CHEST / THORAX: Diaphragm > Denervation | HP:0009109 | ||
phenodb:0786 | CHEST / THORAX: Diaphragm > Defect | HP:0009112 | ||
phenodb:0787 | CHEST / THORAX: Diaphragm > Diminished motion | HP:0009113 | ||
phenodb:0788 | CHEST / THORAX: Diaphragm > Eventration | HP:0009110 | T1572 | |
phenodb:0789 | CHEST / THORAX: Diaphragm > Hernia, congenital | HP:0000776 | T1573 | |
phenodb:0790 | CHEST / THORAX: Diaphragm > Hiatal hernia | HP:0002036 | T1495 | |
phenodb:0791 | CHEST / THORAX: Diaphragm > Paralysis | HP:0006597 | T1576 | |
phenodb:0792 | CHEST / THORAX: Diaphragm > Weakness | HP:0009113 | ||
phenodb:0793 | CHEST / THORAX: Diaphragm > Other feature | |||
phenodb:3048 | CHEST / THORAX: Mediastinum | |||
phenodb:3049 | CHEST / THORAX: Mediastinum > Mediastinal lymphadenopathy | HP:0100721 | T1631 | |
phenodb:3616 | CHEST / THORAX: Mediastinum > Other feature | |||
phenodb:0794 | CARDIOVASCULAR: | HP:0001626 | ||
phenodb:0795 | CARDIOVASCULAR: Heart | HP:0001627 | ||
phenodb:0796 | CARDIOVASCULAR: Heart > Structure | |||
phenodb:0797 | CARDIOVASCULAR: Heart > Structure > General | HP:0002564 | T1728 | |
phenodb:0798 | CARDIOVASCULAR: Heart > Structure > General > Atrioventricular canal | HP:0006695 | T1754 | |
phenodb:0799 | CARDIOVASCULAR: Heart > Structure > General > Atrium, single | HP:0011565 | T1731 | |
phenodb:0800 | CARDIOVASCULAR: Heart > Structure > General > Cardiomegaly | HP:0001640 | T1722 | |
phenodb:0801 | CARDIOVASCULAR: Heart > Structure > General > Congenital heart defect, NOS | HP:0002564 | ||
phenodb:0802 | CARDIOVASCULAR: Heart > Structure > General > Dextrocardia | HP:0001651 | T1726 | |
phenodb:3050 | CARDIOVASCULAR: Heart > Structure > General > Ebstein anomaly | HP:0010316 | T1700 | |
phenodb:3051 | CARDIOVASCULAR: Heart > Structure > General > Endocarditis | HP:0100584 | T1771 | |
phenodb:0803 | CARDIOVASCULAR: Heart > Structure > General > Fibroelastosis | HP:0001706 | T1770 | |
phenodb:0804 | CARDIOVASCULAR: Heart > Structure > General > Hypoplastic left heart | HP:0004383 | T1736 | |
phenodb:0805 | CARDIOVASCULAR: Heart > Structure > General > Myocardial fibrosis | HP:0001685 | T1764 | |
phenodb:0806 | CARDIOVASCULAR: Heart > Structure > General > Rhabdomyoma | HP:0009730 | ||
phenodb:0807 | CARDIOVASCULAR: Heart > Structure > General > Right ventricle, double-outlet | HP:0001719 | ||
phenodb:0808 | CARDIOVASCULAR: Heart > Structure > General > Subaortic stenosis | HP:0001682 | T1739 | |
phenodb:0809 | CARDIOVASCULAR: Heart > Structure > General > Tetralogy of Fallot | HP:0001636 | T1744 | |
phenodb:0810 | CARDIOVASCULAR: Heart > Structure > General > Transposition of the great vessels | HP:0001669 | T1743 | |
phenodb:0811 | CARDIOVASCULAR: Heart > Structure > General > Truncus arteriosus | HP:0001660 | T1745 | |
phenodb:0812 | CARDIOVASCULAR: Heart > Structure > General > Ventricle, single | HP:0001750 | T1729 | |
phenodb:0813 | CARDIOVASCULAR: Heart > Structure > General > Other feature | |||
phenodb:0814 | CARDIOVASCULAR: Heart > Structure > Septa | HP:0001671 | T1749 | |
phenodb:0815 | CARDIOVASCULAR: Heart > Structure > Septa > Asymmetric septal hypertrophy | HP:0001670 | ||
phenodb:0816 | CARDIOVASCULAR: Heart > Structure > Septa > Atrial septal defect | HP:0001631 | T1751 | |
phenodb:0817 | CARDIOVASCULAR: Heart > Structure > Septa > Patent foramen ovale | HP:0001655 | T1750 | |
phenodb:3052 | CARDIOVASCULAR: Heart > Structure > Septa > Patent ostium primum | HP:0010445 | T1752 | |
phenodb:0818 | CARDIOVASCULAR: Heart > Structure > Septa > Patent ostium secundum | HP:0001684 | ||
phenodb:0819 | CARDIOVASCULAR: Heart > Structure > Septa > Ventricular septal defect | HP:0001629 | T1753 | |
phenodb:0820 | CARDIOVASCULAR: Heart > Structure > Septa > Other feature | |||
phenodb:0821 | CARDIOVASCULAR: Heart > Structure > Valves | HP:0001654 | T1689 | |
phenodb:0822 | CARDIOVASCULAR: Heart > Structure > Valves > Aortic valve | HP:0001646 | T1707 | |
phenodb:3053 | CARDIOVASCULAR: Heart > Structure > Valves > Aortic valve > Atresia | HP:0010883 | T1713 | |
phenodb:0823 | CARDIOVASCULAR: Heart > Structure > Valves > Aortic valve > Bicuspid | HP:0001647 | ||
phenodb:0824 | CARDIOVASCULAR: Heart > Structure > Valves > Aortic valve > Calcification | HP:0004380 | T1710 | |
phenodb:0825 | CARDIOVASCULAR: Heart > Structure > Valves > Aortic valve > Insufficiency | HP:0001659 | T1705 | |
phenodb:0826 | CARDIOVASCULAR: Heart > Structure > Valves > Aortic valve > Regurgitation | HP:0001659 | ||
phenodb:0827 | CARDIOVASCULAR: Heart > Structure > Valves > Aortic valve > Stenosis | HP:0001650 | T1712 | |
phenodb:0828 | CARDIOVASCULAR: Heart > Structure > Valves > Aortic valve > Other feature | |||
phenodb:0829 | CARDIOVASCULAR: Heart > Structure > Valves > Mitral valve | HP:0001633 | ||
phenodb:3054 | CARDIOVASCULAR: Heart > Structure > Valves > Mitral valve > Atresia | HP:0011560 | T1696 | |
phenodb:0830 | CARDIOVASCULAR: Heart > Structure > Valves > Mitral valve > Insufficiency | HP:0001653 | T1693 | |
phenodb:0831 | CARDIOVASCULAR: Heart > Structure > Valves > Mitral valve > Prolapse | HP:0001634 | T1692 | |
phenodb:0832 | CARDIOVASCULAR: Heart > Structure > Valves > Mitral valve > Regurgitation | HP:0001653 | ||
phenodb:3055 | CARDIOVASCULAR: Heart > Structure > Valves > Mitral valve > Stenosis | HP:0001718 | T1697 | |
phenodb:0833 | CARDIOVASCULAR: Heart > Structure > Valves > Mitral valve > Other feature | |||
phenodb:0834 | CARDIOVASCULAR: Heart > Structure > Valves > Pulmonary valve | HP:0001641 | T1714 | |
phenodb:0835 | CARDIOVASCULAR: Heart > Structure > Valves > Pulmonary valve > Absent | HP:0005134 | T1716 | |
phenodb:0836 | CARDIOVASCULAR: Heart > Structure > Valves > Pulmonary valve > Atresia | HP:0010882 | T1717 | |
phenodb:0837 | CARDIOVASCULAR: Heart > Structure > Valves > Pulmonary valve > Bicuspid | HP:0005182 | T1718 | |
phenodb:3056 | CARDIOVASCULAR: Heart > Structure > Valves > Pulmonary valve > Insufficiency | HP:0010444 | T1715 | |
phenodb:0838 | CARDIOVASCULAR: Heart > Structure > Valves > Pulmonary valve > Stenosis | HP:0001642 | T1747 | |
phenodb:0839 | CARDIOVASCULAR: Heart > Structure > Valves > Pulmonary valve > Other feature | |||
phenodb:0840 | CARDIOVASCULAR: Heart > Structure > Valves > Tricuspid valve | HP:0001702 | ||
phenodb:3057 | CARDIOVASCULAR: Heart > Structure > Valves > Tricuspid valve > Atresia | HP:0011662 | T1703 | |
phenodb:3058 | CARDIOVASCULAR: Heart > Structure > Valves > Tricuspid valve > Insufficiency | HP:0005180 | T1698 | |
phenodb:0841 | CARDIOVASCULAR: Heart > Structure > Valves > Tricuspid valve > Prolapse | HP:0001704 | T1699 | |
phenodb:0842 | CARDIOVASCULAR: Heart > Structure > Valves > Tricuspid valve > Regurgitation | HP:0005180 | ||
phenodb:3059 | CARDIOVASCULAR: Heart > Structure > Valves > Tricuspid valve > Stenosis | HP:0010446 | T1704 | |
phenodb:0843 | CARDIOVASCULAR: Heart > Structure > Valves > Tricuspid valve > Other feature | |||
phenodb:0844 | CARDIOVASCULAR: Heart > Structure > Ventricles | |||
phenodb:0845 | CARDIOVASCULAR: Heart > Structure > Ventricles > Hypertrophy | HP:0001714 | ||
phenodb:0846 | CARDIOVASCULAR: Heart > Structure > Ventricles > Hypertrophy > Left | HP:0001712 | T1724 | |
phenodb:0847 | CARDIOVASCULAR: Heart > Structure > Ventricles > Hypertrophy > Right | HP:0001667 | T1725 | |
phenodb:0848 | CARDIOVASCULAR: Heart > Structure > Ventricles > Noncompaction | HP:0012817 | T1758 | |
phenodb:0849 | CARDIOVASCULAR: Heart > Structure > Ventricles > Noncompaction > Left | HP:0011664 | ||
phenodb:0850 | CARDIOVASCULAR: Heart > Structure > Ventricles > Noncompaction > Right | HP:0012816 | ||
phenodb:0851 | CARDIOVASCULAR: Heart > Structure > Ventricles > Fibrofatty replacement of right ventricular myocardium | |||
phenodb:2875 | CARDIOVASCULAR: Heart > Structure > Ventricles > Other feature | |||
phenodb:3060 | CARDIOVASCULAR: Heart > Structure > Pericardium | HP:0001697 | T1766 | |
phenodb:3061 | CARDIOVASCULAR: Heart > Structure > Pericardium > Constrictive pericarditis | HP:0002563 | T1768 | |
phenodb:3062 | CARDIOVASCULAR: Heart > Structure > Pericardium > Non-constrictive pericarditis | HP:0001701 | ||
phenodb:3617 | CARDIOVASCULAR: Heart > Structure > Pericardium > Other feature | |||
phenodb:0852 | CARDIOVASCULAR: Heart > Function | |||
phenodb:0853 | CARDIOVASCULAR: Heart > Function > Angina | HP:0001681 | ||
phenodb:3063 | CARDIOVASCULAR: Heart > Function > Arrhythmogenic right ventricular cardiomyopathy | |||
phenodb:0854 | CARDIOVASCULAR: Heart > Function > Cardiomyopathy | HP:0001638 | T1762 | |
phenodb:0855 | CARDIOVASCULAR: Heart > Function > Cardiomyopathy, dilated | HP:0001644 | T1756 | |
phenodb:0856 | CARDIOVASCULAR: Heart > Function > Cardiomyopathy, hypertrophic | HP:0001639 | T1757 | |
phenodb:0857 | CARDIOVASCULAR: Heart > Function > Cardiomyopathy, right ventricular | HP:0011663 | T1760 | |
phenodb:0858 | CARDIOVASCULAR: Heart > Function > Congestive heart failure | HP:0001635 | T1813 | |
phenodb:0859 | CARDIOVASCULAR: Heart > Function > Cor pulmonale | HP:0001648 | ||
phenodb:0860 | CARDIOVASCULAR: Heart > Function > Heart failure | HP:0001635 | ||
phenodb:0861 | CARDIOVASCULAR: Heart > Function > Myocardial infarction | HP:0001658 | T1810 | |
phenodb:0862 | CARDIOVASCULAR: Heart > Function > Myocarditis | HP:0012819 | ||
phenodb:0863 | CARDIOVASCULAR: Heart > Function > Pericardial effusion | HP:0001698 | T1765 | |
phenodb:0864 | CARDIOVASCULAR: Heart > Function > Pericarditis | HP:0001701 | T1767 | |
phenodb:2828 | CARDIOVASCULAR: Heart > Function > Rhythm | HP:0003115 | T1797 | |
phenodb:3066 | CARDIOVASCULAR: Heart > Function > Rhythm > Angina pectoris | HP:0001681 | T1811 | |
phenodb:2829 | CARDIOVASCULAR: Heart > Function > Rhythm > Arrhythmia | HP:0011675 | T1791 | |
phenodb:2830 | CARDIOVASCULAR: Heart > Function > Rhythm > Atrial fibrillation | HP:0005110 | T1796 | |
phenodb:2831 | CARDIOVASCULAR: Heart > Function > Rhythm > Atrioventricular block | HP:0001678 | ||
phenodb:2832 | CARDIOVASCULAR: Heart > Function > Rhythm > Bradycardia | HP:0001662 | T1800 | |
phenodb:3064 | CARDIOVASCULAR: Heart > Function > Rhythm > Bundle branch block, left | HP:0011713 | T1808 | |
phenodb:2833 | CARDIOVASCULAR: Heart > Function > Rhythm > Bundle branch block, right | HP:0011712 | T1809 | |
phenodb:3068 | CARDIOVASCULAR: Heart > Function > Rhythm > Cardiac arrest | HP:0001695 | T1815 | |
phenodb:2834 | CARDIOVASCULAR: Heart > Function > Rhythm > Cardiac conduction defects, NOS | HP:0011675 | ||
phenodb:3067 | CARDIOVASCULAR: Heart > Function > Rhythm > Circulatory collapse | |||
phenodb:2835 | CARDIOVASCULAR: Heart > Function > Rhythm > Heart block | HP:0001678 | T1807 | |
phenodb:2836 | CARDIOVASCULAR: Heart > Function > Rhythm > Palpitations | HP:0001962 | T1803 | |
phenodb:3682 | CARDIOVASCULAR: Heart > Function > Rhythm > Paroxysmal supraventricular tachycardia | HP:0004763 | T6004 | |
phenodb:2837 | CARDIOVASCULAR: Heart > Function > Rhythm > Prolonged QT interval on EKG | HP:0001657 | T1798 | |
phenodb:3065 | CARDIOVASCULAR: Heart > Function > Rhythm > Short QT interval on EKG | HP:0001657 | ||
phenodb:2838 | CARDIOVASCULAR: Heart > Function > Rhythm > Sudden cardiac death | HP:0001645 | T1816 | |
phenodb:2839 | CARDIOVASCULAR: Heart > Function > Rhythm > Supraventricular tachycardia | HP:0004755 | T1802 | |
phenodb:2840 | CARDIOVASCULAR: Heart > Function > Rhythm > Syncope | HP:0001279 | T1812 | |
phenodb:2841 | CARDIOVASCULAR: Heart > Function > Rhythm > Tachycardia | HP:0001649 | T1794 | |
phenodb:2842 | CARDIOVASCULAR: Heart > Function > Rhythm > Torsade de pointes | HP:0001664 | T1801 | |
phenodb:2843 | CARDIOVASCULAR: Heart > Function > Rhythm > Ventricular fibrillation | HP:0001663 | T1795 | |
phenodb:2844 | CARDIOVASCULAR: Heart > Function > Rhythm > Ventricular tachycardia | HP:0004756 | T1793 | |
phenodb:2845 | CARDIOVASCULAR: Heart > Function > Rhythm > Wolff-Parkinson-White syndrome | HP:0001716 | T1804 | |
phenodb:2846 | CARDIOVASCULAR: Heart > Function > Rhythm > Other feature | |||
phenodb:0865 | CARDIOVASCULAR: Heart > Function > Other feature | |||
phenodb:0866 | CARDIOVASCULAR: Vascular | HP:0002597 | ||
phenodb:0867 | CARDIOVASCULAR: Vascular > Aneurysm, abdominal aortic | HP:0004953 | T1776 | |
phenodb:3069 | CARDIOVASCULAR: Vascular > Aneurysm, aortic | HP:0004942 | ||
phenodb:0868 | CARDIOVASCULAR: Vascular > Aneurysm, aortic root | HP:0002616 | T1775 | |
phenodb:0869 | CARDIOVASCULAR: Vascular > Aneurysm, ascending aortic | HP:0002631 | ||
phenodb:0870 | CARDIOVASCULAR: Vascular > Aneurysm, cerebral / intracranial | HP:0004944 | T2152 | |
phenodb:0871 | CARDIOVASCULAR: Vascular > Aneurysm, pulmonary artery | HP:0004937 | T1748 | |
phenodb:0872 | CARDIOVASCULAR: Vascular > Aneurysm, thoracic aortic | HP:0012727 | T1779 | |
phenodb:3070 | CARDIOVASCULAR: Vascular > Aneurysm, vein of Galen | |||
phenodb:0873 | CARDIOVASCULAR: Vascular > Aneurysm, other | |||
phenodb:0874 | CARDIOVASCULAR: Vascular > Aneurysm, other > Specify location | |||
phenodb:3071 | CARDIOVASCULAR: Vascular > Interrupted aortic arch | HP:0011611 | T1737 | |
phenodb:3072 | CARDIOVASCULAR: Vascular > Double aortic arch | HP:0011590 | T2919 | |
phenodb:0875 | CARDIOVASCULAR: Vascular > Aortic arch, right sided | HP:0012020 | T1733 | |
phenodb:3073 | CARDIOVASCULAR: Vascular > Overriding aorta | HP:0002623 | T1742 | |
phenodb:0876 | CARDIOVASCULAR: Vascular > Aortic coarctation | HP:0001680 | T1738 | |
phenodb:3670 | CARDIOVASCULAR: Vascular > Aortic dissection | HP:0002647 | T1777 | |
phenodb:3074 | CARDIOVASCULAR: Vascular > Arterial stenosis | HP:0100545 | T1826 | |
phenodb:3075 | CARDIOVASCULAR: Vascular > Arterial rupture | HP:0005294 | T1835 | |
phenodb:0877 | CARDIOVASCULAR: Vascular > Arterial tortuosity | HP:0005116 | ||
phenodb:0878 | CARDIOVASCULAR: Vascular > Arteriosclerosis | HP:0002634 | ||
phenodb:3076 | CARDIOVASCULAR: Vascular > Arteriovenous fistula of peripheral vessels | |||
phenodb:0879 | CARDIOVASCULAR: Vascular > Arteriovenous malformation | HP:0100026 | T1786 | |
phenodb:0880 | CARDIOVASCULAR: Vascular > Arteriovenous malformation > Specify location | |||
phenodb:3077 | CARDIOVASCULAR: Vascular > Arteritis | HP:0012089 | T1838 | |
phenodb:3079 | CARDIOVASCULAR: Vascular > Atheromatosis | HP:0002635 | T1831 | |
phenodb:0881 | CARDIOVASCULAR: Vascular > Atherosclerosis, premature | HP:0002621 | T6007 | |
phenodb:2827 | CARDIOVASCULAR: Vascular > Calcification | HP:0004934 | ||
phenodb:3087 | CARDIOVASCULAR: Vascular > Capillary malformation | |||
phenodb:3080 | CARDIOVASCULAR: Vascular > Carotid artery anomaly | HP:0005344 | ||
phenodb:0882 | CARDIOVASCULAR: Vascular > Cerebral ischemia | HP:0002637 | T2150 | |
phenodb:3081 | CARDIOVASCULAR: Vascular > Cerebral vasculature anomaly | HP:0100659 | T2149 | |
phenodb:0883 | CARDIOVASCULAR: Vascular > Claudication | HP:0004417 | T2391 | |
phenodb:0884 | CARDIOVASCULAR: Vascular > Coronary artery disease | HP:0001677 | ||
phenodb:2847 | CARDIOVASCULAR: Vascular > Dissection, without aneurysm | |||
phenodb:2848 | CARDIOVASCULAR: Vascular > Dissection, without aneurysm > Specify location | |||
phenodb:3082 | CARDIOVASCULAR: Vascular > Fibromuscular dysplasia | HP:0005313 | ||
phenodb:0885 | CARDIOVASCULAR: Vascular > Hypertension | HP:0000822 | T1818 | |
phenodb:0886 | CARDIOVASCULAR: Vascular > Hypotension | HP:0002615 | T1820 | |
phenodb:0887 | CARDIOVASCULAR: Vascular > Orthostatic hypotension | HP:0001278 | ||
phenodb:0888 | CARDIOVASCULAR: Vascular > Patent ductus arteriosus | HP:0001643 | T1755 | |
phenodb:3083 | CARDIOVASCULAR: Vascular > Pulmonary artery atresia | HP:0004935 | T1746 | |
phenodb:0889 | CARDIOVASCULAR: Vascular > Pulmonary artery stenosis | HP:0004415 | ||
phenodb:0890 | CARDIOVASCULAR: Vascular > Pulmonary hypertension | HP:0002092 | T1668 | |
phenodb:3084 | CARDIOVASCULAR: Vascular > Pulmonary veins anomaly | HP:0011718 | T1781 | |
phenodb:0891 | CARDIOVASCULAR: Vascular > Supravalvular aortic stenosis | HP:0004381 | T1711 | |
phenodb:0892 | CARDIOVASCULAR: Vascular > Telangiectasia | HP:0001009 | ||
phenodb:0893 | CARDIOVASCULAR: Vascular > Telangiectasia > Specify location | |||
phenodb:0894 | CARDIOVASCULAR: Vascular > Thrombosis, arterial | HP:0004420 | T1824 | |
phenodb:0895 | CARDIOVASCULAR: Vascular > Thrombosis, deep vein | HP:0002625 | T1828 | |
phenodb:0896 | CARDIOVASCULAR: Vascular > Thrombosis, pulmonary | HP:0002204 | ||
phenodb:3085 | CARDIOVASCULAR: Vascular > Thrombosis, venous | HP:0004936 | T1827 | |
phenodb:0897 | CARDIOVASCULAR: Vascular > Total anomalous pulmonary venous return (TAPVR) | HP:0005160 | T1734 | |
phenodb:3086 | CARDIOVASCULAR: Vascular > Vascular malformation | |||
phenodb:0898 | CARDIOVASCULAR: Vascular > Vascular ring | HP:0010775 | T1790 | |
phenodb:3078 | CARDIOVASCULAR: Vascular > Vasculitis | HP:0002633 | T1839 | |
phenodb:0899 | CARDIOVASCULAR: Vascular > Veins, prominent superficial | HP:0001015 | ||
phenodb:0900 | CARDIOVASCULAR: Vascular > Veins, varicose | HP:0002619 | T1837 | |
phenodb:3089 | CARDIOVASCULAR: Vascular > Venous insufficiency | HP:0005293 | T1836 | |
phenodb:3088 | CARDIOVASCULAR: Vascular > Venous malformation | HP:0012721 | T1789 | |
phenodb:2876 | CARDIOVASCULAR: Vascular > Other feature | |||
phenodb:0901 | RESPIRATORY: | HP:0002086 | ||
phenodb:0902 | RESPIRATORY: General function | |||
phenodb:0903 | RESPIRATORY: General function > Abnormal respiratory patterns | HP:0002793 | T1655 | |
phenodb:0904 | RESPIRATORY: General function > Apnea | HP:0002104 | ||
phenodb:0905 | RESPIRATORY: General function > Ciliary dyskinesia | HP:0012265 | T2037 | |
phenodb:0906 | RESPIRATORY: General function > Cyanosis | HP:0000961 | ||
phenodb:0907 | RESPIRATORY: General function > Cough | HP:0012735 | T1664 | |
phenodb:0908 | RESPIRATORY: General function > Dyspnea | HP:0002094 | T1651 | |
phenodb:0909 | RESPIRATORY: General function > Hyperpnea (deep) | HP:0005941 | ||
phenodb:0910 | RESPIRATORY: General function > Intermittent episodes of respiratory insufficiency due to muscle weakness | HP:0004889 | ||
phenodb:0911 | RESPIRATORY: General function > Respiratory distress | HP:0002098 | ||
phenodb:0912 | RESPIRATORY: General function > Respiratory distress, neonatal | HP:0002643 | ||
phenodb:0913 | RESPIRATORY: General function > Respiratory failure | HP:0002093 | ||
phenodb:0914 | RESPIRATORY: General function > Respiratory paralysis | HP:0002203 | ||
phenodb:0915 | RESPIRATORY: General function > Recurrent respiratory infections | HP:0002205 | ||
phenodb:0916 | RESPIRATORY: General function > Sleep apnea | HP:0010535 | T1656 | |
phenodb:0917 | RESPIRATORY: General function > Sleep apnea > Central | HP:0010536 | T1658 | |
phenodb:0918 | RESPIRATORY: General function > Sleep apnea > Obstructive | HP:0002870 | T1657 | |
phenodb:0919 | RESPIRATORY: General function > Sleep apnea > Other feature | |||
phenodb:0920 | RESPIRATORY: General function > Sudden episodic apnea | HP:0002882 | ||
phenodb:0921 | RESPIRATORY: General function > Tachypnea (fast) | HP:0002789 | ||
phenodb:2877 | RESPIRATORY: General function > Other feature | |||
phenodb:0922 | RESPIRATORY: Nasopharynx | HP:0001739 | ||
phenodb:0923 | RESPIRATORY: Nasopharynx > Choanal atresia | HP:0000453 | ||
phenodb:0924 | RESPIRATORY: Nasopharynx > Choanal stenosis | HP:0000452 | ||
phenodb:2849 | RESPIRATORY: Nasopharynx > Sinusitis, chronic | HP:0011109 | T0461 | |
phenodb:3090 | RESPIRATORY: Nasopharynx > Velopharyngeal insufficiency | HP:0000220 | T1414 | |
phenodb:0925 | RESPIRATORY: Nasopharynx > Other feature | |||
phenodb:3091 | RESPIRATORY: Pharynx | HP:0000600 | T1415 | |
phenodb:3092 | RESPIRATORY: Pharynx > Tonsil anomaly | HP:0100765 | T1418 | |
phenodb:3618 | RESPIRATORY: Pharynx > Other feature | |||
phenodb:0926 | RESPIRATORY: Larynx | HP:0001600 | ||
phenodb:0927 | RESPIRATORY: Larynx > Epiglottis | HP:0005483 | T1580 | |
phenodb:0928 | RESPIRATORY: Larynx > Epiglottis > Abnormality of the aryepiglottic fold | HP:0008744 | ||
phenodb:0929 | RESPIRATORY: Larynx > Epiglottis > Aplasia | HP:0008753 | ||
phenodb:0930 | RESPIRATORY: Larynx > Epiglottis > Bifid | HP:0010564 | ||
phenodb:0931 | RESPIRATORY: Larynx > Epiglottis > Hypoplasia | HP:0005349 | ||
phenodb:0932 | RESPIRATORY: Larynx > Epiglottis > Other feature | |||
phenodb:0933 | RESPIRATORY: Larynx > Larynx | HP:0001600 | T1589 | |
phenodb:0934 | RESPIRATORY: Larynx > Larynx > Anteroposteriorly shortened | HP:0005956 | ||
phenodb:0935 | RESPIRATORY: Larynx > Larynx > Calcifications | HP:0008754 | T1591 | |
phenodb:0936 | RESPIRATORY: Larynx > Larynx > Cartilage abnormalities | HP:0008747 | ||
phenodb:0937 | RESPIRATORY: Larynx > Larynx > Cartilaginous ossification | HP:0008747 | ||
phenodb:0938 | RESPIRATORY: Larynx > Larynx > Cleft | HP:0008751 | T1604 | |
phenodb:0939 | RESPIRATORY: Larynx > Larynx > Cyst | HP:0100640 | T1601 | |
phenodb:3093 | RESPIRATORY: Larynx > Larynx > Edema | HP:0012027 | ||
phenodb:0940 | RESPIRATORY: Larynx > Larynx > Hypoplasia | HP:0008749 | ||
phenodb:0941 | RESPIRATORY: Larynx > Larynx > Laryngomalacia | HP:0001601 | T1592 | |
phenodb:0942 | RESPIRATORY: Larynx > Larynx > Obstruction | HP:0005945 | ||
phenodb:0943 | RESPIRATORY: Larynx > Larynx > Partial atresia | HP:0005950 | ||
phenodb:0944 | RESPIRATORY: Larynx > Larynx > Stenosis | HP:0001602 | ||
phenodb:0945 | RESPIRATORY: Larynx > Larynx > Stridor | HP:0010307 | T1676 | |
phenodb:0946 | RESPIRATORY: Larynx > Larynx > Subglottic stenosis | HP:0001607 | T1600 | |
phenodb:0947 | RESPIRATORY: Larynx > Larynx > Other feature | |||
phenodb:0948 | RESPIRATORY: Larynx > Vocal cord | HP:0008777 | T1582 | |
phenodb:0949 | RESPIRATORY: Larynx > Vocal cord > Bowing | HP:0008756 | ||
phenodb:0950 | RESPIRATORY: Larynx > Vocal cord > Incomplete adduction | HP:0005934 | ||
phenodb:0951 | RESPIRATORY: Larynx > Vocal cord > Paralysis | HP:0001605 | ||
phenodb:0952 | RESPIRATORY: Larynx > Vocal cord > Paralysis > Unilateral | HP:0008757 | T1584 | |
phenodb:0953 | RESPIRATORY: Larynx > Vocal cord > Paralysis > Bilateral | HP:0012820 | T2932 | |
phenodb:0954 | RESPIRATORY: Larynx > Vocal cord > Paresis | HP:0001604 | ||
phenodb:0955 | RESPIRATORY: Larynx > Vocal cord > Paresis > Unilateral | HP:0012821 | ||
phenodb:0956 | RESPIRATORY: Larynx > Vocal cord > Paresis > Bilateral | HP:0012822 | ||
phenodb:2878 | RESPIRATORY: Larynx > Vocal cord > Other feature | |||
phenodb:0957 | RESPIRATORY: Airways | |||
phenodb:0958 | RESPIRATORY: Airways > Structure | |||
phenodb:0959 | RESPIRATORY: Airways > Structure > Ectopic respiratory mucosa | HP:0100241 | ||
phenodb:0960 | RESPIRATORY: Airways > Structure > Trachea | HP:0002778 | ||
phenodb:0961 | RESPIRATORY: Airways > Structure > Trachea > Anomalous tracheal cartilage | HP:0004468 | ||
phenodb:0962 | RESPIRATORY: Airways > Structure > Trachea > Atresia | HP:0100682 | T1611 | |
phenodb:0963 | RESPIRATORY: Airways > Structure > Trachea > Calcification | HP:0002787 | T1607 | |
phenodb:0964 | RESPIRATORY: Airways > Structure > Trachea > Cartilagenous | HP:0005347 | ||
phenodb:0965 | RESPIRATORY: Airways > Structure > Trachea > Diverticulosis | HP:0006509 | ||
phenodb:0966 | RESPIRATORY: Airways > Structure > Trachea > Stenosis | HP:0002777 | T1610 | |
phenodb:0967 | RESPIRATORY: Airways > Structure > Trachea > Tracheoesophageal fistula | HP:0002575 | ||
phenodb:0968 | RESPIRATORY: Airways > Structure > Trachea > Tracheomalacia | HP:0002779 | T1614 | |
phenodb:0969 | RESPIRATORY: Airways > Structure > Trachea > Tracheomegaly | HP:0010778 | ||
phenodb:0970 | RESPIRATORY: Airways > Structure > Trachea > Other feature | |||
phenodb:0971 | RESPIRATORY: Airways > Structure > Bronchi | HP:0002109 | ||
phenodb:0972 | RESPIRATORY: Airways > Structure > Bronchi > Bronchial cartilage hypoplasia | HP:0006539 | ||
phenodb:0973 | RESPIRATORY: Airways > Structure > Bronchi > Bronchiectasis | HP:0002110 | T1663 | |
phenodb:3095 | RESPIRATORY: Airways > Structure > Bronchi > Bronchiolitis | HP:0011950 | T1683 | |
phenodb:0974 | RESPIRATORY: Airways > Structure > Bronchi > Chronic Bronchitis | HP:0004469 | T1685 | |
phenodb:0975 | RESPIRATORY: Airways > Structure > Bronchi > Bronchodysplasia | HP:0006533 | ||
phenodb:3094 | RESPIRATORY: Airways > Structure > Bronchi > Bronchogenic cyst | HP:0100730 | T1669 | |
phenodb:0976 | RESPIRATORY: Airways > Structure > Bronchi > Bronchomalacia | HP:0002780 | T1615 | |
phenodb:0977 | RESPIRATORY: Airways > Structure > Bronchi > Bronchomegaly | HP:0010777 | ||
phenodb:0978 | RESPIRATORY: Airways > Structure > Bronchi > Other feature | |||
phenodb:0979 | RESPIRATORY: Airways > Function | |||
phenodb:0980 | RESPIRATORY: Airways > Function > Aspiration | HP:0002835 | ||
phenodb:0981 | RESPIRATORY: Airways > Function > Asthma & reactive airways disease | HP:0002099 | T1662 | |
phenodb:0982 | RESPIRATORY: Airways > Function > Upper airway obstruction | HP:0002781 | T0458 | |
phenodb:0983 | RESPIRATORY: Airways > Function > Upper respiratory tract infections | HP:0002788 | T6010 | |
phenodb:0984 | RESPIRATORY: Airways > Function > Other feature | |||
phenodb:0985 | RESPIRATORY: Lung | HP:0002088 | ||
phenodb:0986 | RESPIRATORY: Lung > Function | |||
phenodb:0987 | RESPIRATORY: Lung > Function > Alveolar proteinosis | HP:0006517 | ||
phenodb:3619 | RESPIRATORY: Lung > Function > Atelectasis | HP:0100750 | T1667 | |
phenodb:3103 | RESPIRATORY: Lung > Function > Chronic obstructive lung disease | HP:0006510 | T1687 | |
phenodb:0988 | RESPIRATORY: Lung > Function > Desquamative interstitial pneumonitis | HP:0005942 | ||
phenodb:0989 | RESPIRATORY: Lung > Function > Emphysema | HP:0002097 | T1661 | |
phenodb:3096 | RESPIRATORY: Lung > Function > Hemoptysis | HP:0002105 | T1665 | |
phenodb:0990 | RESPIRATORY: Lung > Function > Interstitial lung disease | HP:0006530 | T1681 | |
phenodb:3100 | RESPIRATORY: Lung > Function > Lung infiltration | HP:0002113 | T1630 | |
phenodb:3097 | RESPIRATORY: Lung > Function > Obstructive lung disease | HP:0006536 | T1686 | |
phenodb:0991 | RESPIRATORY: Lung > Function > Pneumonias (aka Lower respiratory tract infections) | HP:0002783 | T1647 | |
phenodb:3099 | RESPIRATORY: Lung > Function > Pulmonary edema | HP:0100598 | T1632 | |
phenodb:3098 | RESPIRATORY: Lung > Function > Pulmonary fibrosis | HP:0002206 | T1633 | |
phenodb:3101 | RESPIRATORY: Lung > Function > Respiratory acidosis | HP:0005972 | T1642 | |
phenodb:3102 | RESPIRATORY: Lung > Function > Respiratory alkalosis | HP:0001950 | T1644 | |
phenodb:0992 | RESPIRATORY: Lung > Function > Respiratory failure | HP:0002093 | ||
phenodb:0993 | RESPIRATORY: Lung > Function > Respiratory insufficiency | HP:0002093 | T1641 | |
phenodb:0994 | RESPIRATORY: Lung > Function > Restrictive lung disease | HP:0002091 | T1682 | |
phenodb:0995 | RESPIRATORY: Lung > Function > Other feature | |||
phenodb:0996 | RESPIRATORY: Lung > Structure | |||
phenodb:0997 | RESPIRATORY: Lung > Structure > Lung | HP:0002088 | T1619 | |
phenodb:0998 | RESPIRATORY: Lung > Structure > Lung > Arteriovenous malformation | HP:0006548 | T1635 | |
phenodb:0999 | RESPIRATORY: Lung > Structure > Lung > Lung lobation, abnormal | HP:0002101 | T1624 | |
phenodb:1000 | RESPIRATORY: Lung > Structure > Lung > Lymphangiomyomatosis | HP:0012798 | ||
phenodb:3104 | RESPIRATORY: Lung > Structure > Lung > Pulmonary agenesis | HP:0005944 | T1622 | |
phenodb:1001 | RESPIRATORY: Lung > Structure > Lung > Pulmonary embolism | HP:0002204 | T1825 | |
phenodb:1002 | RESPIRATORY: Lung > Structure > Lung > Pulmonary fibrosis / Interstitial fibrosis | HP:0002206 | ||
phenodb:1003 | RESPIRATORY: Lung > Structure > Lung > Pulmonary hypoplasia / Lung hypoplasia | HP:0002089 | T1621 | |
phenodb:3105 | RESPIRATORY: Lung > Structure > Lung > Pulmonary sequestration | HP:0100632 | T1623 | |
phenodb:1004 | RESPIRATORY: Lung > Structure > Lung > Other feature | |||
phenodb:1005 | RESPIRATORY: Lung > Structure > Pleura | HP:0002103 | T1625 | |
phenodb:3106 | RESPIRATORY: Lung > Structure > Pleura > Chylothorax | HP:0010310 | T1627 | |
phenodb:1006 | RESPIRATORY: Lung > Structure > Pleura > Pleural effusion | HP:0002202 | T1628 | |
phenodb:1007 | RESPIRATORY: Lung > Structure > Pleura > Pleuritis | HP:0002102 | T1626 | |
phenodb:1008 | RESPIRATORY: Lung > Structure > Pleura > Pneumothorax | HP:0002107 | T1637 | |
phenodb:1009 | RESPIRATORY: Lung > Structure > Pleura > Other feature | |||
phenodb:1010 | ABDOMEN: | HP:0001438 | ||
phenodb:1011 | ABDOMEN: General / External abnormalities | HP:0001438 | ||
phenodb:1012 | ABDOMEN: General / External abnormalities > Structure | |||
phenodb:3107 | ABDOMEN: General / External abnormalities > Structure > Abdominal wall abnormality | HP:0004298 | T0871 | |
phenodb:1013 | ABDOMEN: General / External abnormalities > Structure > Abdominal wall musculature diminished | HP:0005247 | T0880 | |
phenodb:3108 | ABDOMEN: General / External abnormalities > Structure > Aplasia of the abdominal wall musculature | HP:0005199 | T0881 | |
phenodb:3109 | ABDOMEN: General / External abnormalities > Structure > Hernia of the abdominal wall | HP:0004299 | T0883 | |
phenodb:3110 | ABDOMEN: General / External abnormalities > Structure > Cloacal exstrophy | HP:0010475 | T1886 | |
phenodb:1014 | ABDOMEN: General / External abnormalities > Structure > Diastasis recti | HP:0001540 | T0872 | |
phenodb:1015 | ABDOMEN: General / External abnormalities > Structure > Gastroschisis | HP:0001543 | T0878 | |
phenodb:1016 | ABDOMEN: General / External abnormalities > Structure > Inguinal hernia | HP:0000023 | ||
phenodb:1017 | ABDOMEN: General / External abnormalities > Structure > Meckel diverticulum | HP:0002245 | T1465 | |
phenodb:1018 | ABDOMEN: General / External abnormalities > Structure > Omphalocele | HP:0001539 | T0877 | |
phenodb:3111 | ABDOMEN: General / External abnormalities > Structure > Patent urachus | HP:0010479 | T0889 | |
phenodb:3112 | ABDOMEN: General / External abnormalities > Structure > Protuberant | HP:0001538 | T0874 | |
phenodb:1019 | ABDOMEN: General / External abnormalities > Structure > Situs inversus | HP:0003363 | T1462 | |
phenodb:1020 | ABDOMEN: General / External abnormalities > Structure > Umbilical hernia | HP:0001537 | T0888 | |
phenodb:1021 | ABDOMEN: General / External abnormalities > Structure > Other feature | |||
phenodb:1022 | ABDOMEN: General / External abnormalities > Function | |||
phenodb:1024 | ABDOMEN: General / External abnormalities > Function > Abdominal distention | HP:0003270 | T0875 | |
phenodb:1023 | ABDOMEN: General / External abnormalities > Function > Abdominal pain | HP:0002027 | T1501 | |
phenodb:1025 | ABDOMEN: General / External abnormalities > Function > Anorexia | HP:0002039 | ||
phenodb:1026 | ABDOMEN: General / External abnormalities > Function > Ascites | HP:0001541 | T1484 | |
phenodb:1027 | ABDOMEN: General / External abnormalities > Function > Feeding difficulties / Poor feeding | HP:0011968 | T1486 | |
phenodb:1028 | ABDOMEN: General / External abnormalities > Function > Malnutrition | HP:0004395 | T2824 | |
phenodb:1029 | ABDOMEN: General / External abnormalities > Function > Nausea | HP:0002018 | T1491 | |
phenodb:1030 | ABDOMEN: General / External abnormalities > Function > Peritonitis | HP:0002586 | T1522 | |
phenodb:1031 | ABDOMEN: General / External abnormalities > Function > Protein avoidance | HP:0002038 | ||
phenodb:3113 | ABDOMEN: General / External abnormalities > Function > Weakness of abdominal walls | HP:0009023 | T0879 | |
phenodb:1032 | ABDOMEN: General / External abnormalities > Function > Other feature | |||
phenodb:1033 | ABDOMEN: Gastrointestinal Tract | HP:0012718 | T1420 | |
phenodb:1034 | ABDOMEN: Gastrointestinal Tract > Esophagus | HP:0002031 | ||
phenodb:1035 | ABDOMEN: Gastrointestinal Tract > Esophagus > Structure | HP:0002031 | T1421 | |
phenodb:1036 | ABDOMEN: Gastrointestinal Tract > Esophagus > Structure > Atresia | HP:0002032 | ||
phenodb:3116 | ABDOMEN: Gastrointestinal Tract > Esophagus > Structure > Barrett's esophagus | HP:0100580 | T1426 | |
phenodb:3117 | ABDOMEN: Gastrointestinal Tract > Esophagus > Structure > Diverticulum | HP:0100628 | T1428 | |
phenodb:3118 | ABDOMEN: Gastrointestinal Tract > Esophagus > Structure > Duplication | HP:0100681 | T1429 | |
phenodb:2850 | ABDOMEN: Gastrointestinal Tract > Esophagus > Structure > Eosinophilic esophagitis | |||
phenodb:3114 | ABDOMEN: Gastrointestinal Tract > Esophagus > Structure > Esophagitis | HP:0100633 | T1498 | |
phenodb:1037 | ABDOMEN: Gastrointestinal Tract > Esophagus > Structure > Stricture | HP:0002043 | T1424 | |
phenodb:1039 | ABDOMEN: Gastrointestinal Tract > Esophagus > Structure > Tracheoesophageal fistula | HP:0002575 | T1423 | |
phenodb:1038 | ABDOMEN: Gastrointestinal Tract > Esophagus > Structure > Varices | HP:0002040 | T1499 | |
phenodb:3115 | ABDOMEN: Gastrointestinal Tract > Esophagus > Structure > Web | HP:0100594 | T1425 | |
phenodb:1040 | ABDOMEN: Gastrointestinal Tract > Esophagus > Structure > Other feature | |||
phenodb:1041 | ABDOMEN: Gastrointestinal Tract > Esophagus > Function | |||
phenodb:1042 | ABDOMEN: Gastrointestinal Tract > Esophagus > Function > Achalasia | HP:0002571 | T1427 | |
phenodb:1043 | ABDOMEN: Gastrointestinal Tract > Esophagus > Function > Dysphagia | HP:0002015 | ||
phenodb:1045 | ABDOMEN: Gastrointestinal Tract > Esophagus > Function > Other feature | |||
phenodb:1046 | ABDOMEN: Gastrointestinal Tract > Stomach | HP:0002577 | ||
phenodb:1047 | ABDOMEN: Gastrointestinal Tract > Stomach > Structure | HP:0002577 | T1430 | |
phenodb:3120 | ABDOMEN: Gastrointestinal Tract > Stomach > Structure > Diverticulum | HP:0100808 | T1437 | |
phenodb:2851 | ABDOMEN: Gastrointestinal Tract > Stomach > Structure > Eosinophilic gastritis | |||
phenodb:1048 | ABDOMEN: Gastrointestinal Tract > Stomach > Structure > Gastric ulcer | HP:0002592 | T1494 | |
phenodb:3121 | ABDOMEN: Gastrointestinal Tract > Stomach > Structure > Gastritis | HP:0005263 | T1493 | |
phenodb:3123 | ABDOMEN: Gastrointestinal Tract > Stomach > Structure > Malposition | HP:0100802 | T1436 | |
phenodb:3122 | ABDOMEN: Gastrointestinal Tract > Stomach > Structure > Microgastria | HP:0100841 | T1432 | |
phenodb:1049 | ABDOMEN: Gastrointestinal Tract > Stomach > Structure > Pyloric atresia | HP:0004399 | T1438 | |
phenodb:1050 | ABDOMEN: Gastrointestinal Tract > Stomach > Structure > Pyloric stenosis | HP:0002021 | T1433 | |
phenodb:1051 | ABDOMEN: Gastrointestinal Tract > Stomach > Structure > Other feature | |||
phenodb:1052 | ABDOMEN: Gastrointestinal Tract > Stomach > Function | |||
phenodb:1053 | ABDOMEN: Gastrointestinal Tract > Stomach > Function > Gastroesophageal reflux | HP:0002020 | T1496 | |
phenodb:1054 | ABDOMEN: Gastrointestinal Tract > Stomach > Function > Gastroparesis | HP:0002578 | T1497 | |
phenodb:1055 | ABDOMEN: Gastrointestinal Tract > Stomach > Function > Gastric bleeding | |||
phenodb:1056 | ABDOMEN: Gastrointestinal Tract > Stomach > Function > Hematemesis | HP:0002248 | T1517 | |
phenodb:1057 | ABDOMEN: Gastrointestinal Tract > Stomach > Function > Vomiting | HP:0002013 | T1490 | |
phenodb:1058 | ABDOMEN: Gastrointestinal Tract > Stomach > Function > Other feature | |||
phenodb:1059 | ABDOMEN: Gastrointestinal Tract > Duodenum | HP:0002246 | T1453 | |
phenodb:1060 | ABDOMEN: Gastrointestinal Tract > Duodenum > Atresia | HP:0002247 | T1451 | |
phenodb:1061 | ABDOMEN: Gastrointestinal Tract > Duodenum > Stenosis | HP:0100867 | T1452 | |
phenodb:1062 | ABDOMEN: Gastrointestinal Tract > Duodenum > Ulcer | HP:0002588 | T1492 | |
phenodb:1063 | ABDOMEN: Gastrointestinal Tract > Duodenum > Other feature | |||
phenodb:1064 | ABDOMEN: Gastrointestinal Tract > Small intestine | HP:0002244 | ||
phenodb:1065 | ABDOMEN: Gastrointestinal Tract > Small intestine > Structure | HP:0002244 | T1439 | |
phenodb:3124 | ABDOMEN: Gastrointestinal Tract > Small intestine > Structure > Agenesis | HP:0012739 | T1447 | |
phenodb:1066 | ABDOMEN: Gastrointestinal Tract > Small intestine > Structure > Atresia | HP:0002589 | ||
phenodb:1067 | ABDOMEN: Gastrointestinal Tract > Small intestine > Structure > Crohn disease | HP:0100280 | ||
phenodb:3125 | ABDOMEN: Gastrointestinal Tract > Small intestine > Structure > Diverticulosis | HP:0002256 | T1463 | |
phenodb:3126 | ABDOMEN: Gastrointestinal Tract > Small intestine > Structure > Duplication | HP:0100668 | T1466 | |
phenodb:2852 | ABDOMEN: Gastrointestinal Tract > Small intestine > Structure > Eosinophilic disease | |||
phenodb:3127 | ABDOMEN: Gastrointestinal Tract > Small intestine > Structure > Fistula | HP:0100819 | T1472 | |
phenodb:3128 | ABDOMEN: Gastrointestinal Tract > Small intestine > Structure > Hypoplastic | HP:0004790 | ||
phenodb:3129 | ABDOMEN: Gastrointestinal Tract > Small intestine > Structure > Inflammatory bowel | |||
phenodb:3130 | ABDOMEN: Gastrointestinal Tract > Small intestine > Structure > Lymphangiectasia of the small intestine | HP:0002593 | ||
phenodb:1068 | ABDOMEN: Gastrointestinal Tract > Small intestine > Structure > Malrotation | HP:0004794 | T1469 | |
phenodb:3132 | ABDOMEN: Gastrointestinal Tract > Small intestine > Structure > Polyp | HP:0005266 | ||
phenodb:1069 | ABDOMEN: Gastrointestinal Tract > Small intestine > Structure > Stenosis | HP:0012848 | ||
phenodb:3131 | ABDOMEN: Gastrointestinal Tract > Small intestine > Structure > Telangiectasia of the small intestine | HP:0002604 | ||
phenodb:1070 | ABDOMEN: Gastrointestinal Tract > Small intestine > Structure > Other feature | |||
phenodb:1071 | ABDOMEN: Gastrointestinal Tract > Small intestine > Function | |||
phenodb:1072 | ABDOMEN: Gastrointestinal Tract > Small intestine > Function > Dysmotility | HP:0012850 | ||
phenodb:1073 | ABDOMEN: Gastrointestinal Tract > Small intestine > Function > Hemorrhage | HP:0012849 | ||
phenodb:1074 | ABDOMEN: Gastrointestinal Tract > Small intestine > Function > Ileus | HP:0002595 | T1503 | |
phenodb:1075 | ABDOMEN: Gastrointestinal Tract > Small intestine > Function > Intestinal obstruction | HP:0005214 | T1521 | |
phenodb:1076 | ABDOMEN: Gastrointestinal Tract > Small intestine > Function > Intussusception | HP:0002576 | ||
phenodb:1077 | ABDOMEN: Gastrointestinal Tract > Small intestine > Function > Malabsorption | HP:0002024 | T1506 | |
phenodb:1078 | ABDOMEN: Gastrointestinal Tract > Small intestine > Function > Melena | HP:0002249 | T1516 | |
phenodb:1079 | ABDOMEN: Gastrointestinal Tract > Small intestine > Function > Protein-losing enteropathy | HP:0002243 | T1441 | |
phenodb:1080 | ABDOMEN: Gastrointestinal Tract > Small intestine > Function > Steatorrhea | HP:0002570 | T1505 | |
phenodb:1081 | ABDOMEN: Gastrointestinal Tract > Small intestine > Function > Zollinger-Ellison syndrome | HP:0002044 | ||
phenodb:1082 | ABDOMEN: Gastrointestinal Tract > Small intestine > Function > Other feature | |||
phenodb:1083 | ABDOMEN: Gastrointestinal Tract > Large intestine | HP:0002250 | ||
phenodb:1084 | ABDOMEN: Gastrointestinal Tract > Large intestine > Structure | HP:0002250 | T1440 | |
phenodb:1085 | ABDOMEN: Gastrointestinal Tract > Large intestine > Structure > Atresia | HP:0010448 | T1458 | |
phenodb:3133 | ABDOMEN: Gastrointestinal Tract > Large intestine > Structure > Diverticulosis | HP:0002253 | T1464 | |
phenodb:2853 | ABDOMEN: Gastrointestinal Tract > Large intestine > Structure > Eosinophilic disease | HP:0100280 | ||
phenodb:3134 | ABDOMEN: Gastrointestinal Tract > Large intestine > Structure > Fistula | |||
phenodb:1087 | ABDOMEN: Gastrointestinal Tract > Large intestine > Structure > Hirschsprung disease | HP:0002251 | ||
phenodb:3135 | ABDOMEN: Gastrointestinal Tract > Large intestine > Structure > Inflammatory bowel | HP:0002037 | ||
phenodb:3136 | ABDOMEN: Gastrointestinal Tract > Large intestine > Structure > Lymphangiectasia of the large intestine | HP:0002593 | T1443 | |
phenodb:1088 | ABDOMEN: Gastrointestinal Tract > Large intestine > Structure > Malrotation | HP:0002566 | ||
phenodb:1089 | ABDOMEN: Gastrointestinal Tract > Large intestine > Structure > Megacolon | HP:0002251 | T1461 | |
phenodb:3138 | ABDOMEN: Gastrointestinal Tract > Large intestine > Structure > Microcolon | HP:0004388 | T1457 | |
phenodb:3139 | ABDOMEN: Gastrointestinal Tract > Large intestine > Structure > Polyps | HP:0200063 | T1471 | |
phenodb:1091 | ABDOMEN: Gastrointestinal Tract > Large intestine > Structure > Stenosis | HP:0012851 | ||
phenodb:3137 | ABDOMEN: Gastrointestinal Tract > Large intestine > Structure > Telangiectasia of the large intestine | HP:0002604 | T1444 | |
phenodb:1086 | ABDOMEN: Gastrointestinal Tract > Large intestine > Structure > Ulcerative colitis | HP:0100279 | ||
phenodb:1090 | ABDOMEN: Gastrointestinal Tract > Large intestine > Structure > Villous atrophy | HP:0011473 | T1442 | |
phenodb:3140 | ABDOMEN: Gastrointestinal Tract > Large intestine > Structure > Volvulus | HP:0002580 | ||
phenodb:1092 | ABDOMEN: Gastrointestinal Tract > Large intestine > Structure > Other feature | |||
phenodb:1093 | ABDOMEN: Gastrointestinal Tract > Large intestine > Function | |||
phenodb:1094 | ABDOMEN: Gastrointestinal Tract > Large intestine > Function > Constipation | HP:0002019 | T1510 | |
phenodb:1095 | ABDOMEN: Gastrointestinal Tract > Large intestine > Function > Diarrhea | HP:0002028 | T1504 | |
phenodb:1096 | ABDOMEN: Gastrointestinal Tract > Large intestine > Function > Other feature | |||
phenodb:1097 | ABDOMEN: Gastrointestinal Tract > Rectum / Anus | HP:0012732 | T2916 | |
phenodb:3596 | ABDOMEN: Gastrointestinal Tract > Rectum | HP:0002034 | T1474 | |
phenodb:1098 | ABDOMEN: Gastrointestinal Tract > Rectum > Structure | |||
phenodb:1102 | ABDOMEN: Gastrointestinal Tract > Rectum > Structure > Perirectal abscesses due to immunodeficiency | HP:0005224 | ||
phenodb:3145 | ABDOMEN: Gastrointestinal Tract > Rectum > Structure > Rectal fistula | HP:0100590 | T5932 | |
phenodb:3144 | ABDOMEN: Gastrointestinal Tract > Rectum > Structure > Rectal polyps | HP:0100896 | ||
phenodb:1103 | ABDOMEN: Gastrointestinal Tract > Rectum > Structure > Rectal prolapse | HP:0002035 | T1475 | |
phenodb:3146 | ABDOMEN: Gastrointestinal Tract > Rectum > Structure > Rectoperineal fistula | HP:0004792 | T1477 | |
phenodb:1104 | ABDOMEN: Gastrointestinal Tract > Rectum > Structure > Rectovaginal fistula | HP:0000143 | ||
phenodb:1105 | ABDOMEN: Gastrointestinal Tract > Rectum > Structure > Other feature | |||
phenodb:1106 | ABDOMEN: Gastrointestinal Tract > Rectum > Function | |||
phenodb:3147 | ABDOMEN: Gastrointestinal Tract > Rectum > Function > Encopresis | HP:0002607 | T1508 | |
phenodb:1107 | ABDOMEN: Gastrointestinal Tract > Rectum > Function > Hematochezia | HP:0002573 | T1518 | |
phenodb:1109 | ABDOMEN: Gastrointestinal Tract > Rectum > Function > Other feature | |||
phenodb:3597 | ABDOMEN: Gastrointestinal Tract > Anus | HP:0004378 | ||
phenodb:3598 | ABDOMEN: Gastrointestinal Tract > Anus > Structure | |||
phenodb:3141 | ABDOMEN: Gastrointestinal Tract > Anus > Structure > Anal atresia | HP:0002023 | ||
phenodb:3142 | ABDOMEN: Gastrointestinal Tract > Anus > Structure > Anal fistula | HP:0010447 | T1476 | |
phenodb:1099 | ABDOMEN: Gastrointestinal Tract > Anus > Structure > Anal stenosis | HP:0002025 | T1481 | |
phenodb:3143 | ABDOMEN: Gastrointestinal Tract > Anus > Structure > Anoperineal fistula | HP:0005218 | T2917 | |
phenodb:1100 | ABDOMEN: Gastrointestinal Tract > Anus > Structure > Anus, anteriorly placed | HP:0001545 | T1483 | |
phenodb:1101 | ABDOMEN: Gastrointestinal Tract > Anus > Structure > Anus, imperforate | HP:0002023 | T1480 | |
phenodb:3599 | ABDOMEN: Gastrointestinal Tract > Anus > Structure > Other feature | |||
phenodb:3600 | ABDOMEN: Gastrointestinal Tract > Anus > Function | |||
phenodb:1108 | ABDOMEN: Gastrointestinal Tract > Anus > Function > Incontinence | HP:0002607 | ||
phenodb:3601 | ABDOMEN: Gastrointestinal Tract > Anus > Function > Other feature | |||
phenodb:1110 | ABDOMEN: Liver | HP:0001392 | ||
phenodb:1111 | ABDOMEN: Liver > Structure | |||
phenodb:3148 | ABDOMEN: Liver > Structure > Abcess | HP:0100523 | T1551 | |
phenodb:1112 | ABDOMEN: Liver > Structure > Adenomas | HP:0012028 | ||
phenodb:3150 | ABDOMEN: Liver > Structure > Agenesis | HP:0100839 | T1532 | |
phenodb:3149 | ABDOMEN: Liver > Structure > Anomaly of lobulation | HP:0100752 | T1531 | |
phenodb:1114 | ABDOMEN: Liver > Structure > Bile duct paucity | HP:0006571 | T1529 | |
phenodb:1113 | ABDOMEN: Liver > Structure > Bile duct proliferation | HP:0001408 | ||
phenodb:1115 | ABDOMEN: Liver > Structure > Cirrhosis | HP:0001394 | T1539 | |
phenodb:1116 | ABDOMEN: Liver > Structure > Cysts | HP:0006706 | T1535 | |
phenodb:1117 | ABDOMEN: Liver > Structure > Fibrosis | HP:0001395 | T1533 | |
phenodb:1119 | ABDOMEN: Liver > Structure > Fibrosis > Bridging | HP:0012852 | ||
phenodb:3151 | ABDOMEN: Liver > Structure > Fibrosis > Congenital | HP:0002612 | T2918 | |
phenodb:1118 | ABDOMEN: Liver > Structure > Fibrosis > Periportal | HP:0001405 | ||
phenodb:1120 | ABDOMEN: Liver > Structure > Fibrosis > Other feature | |||
phenodb:1121 | ABDOMEN: Liver > Structure > Steatosis | HP:0001397 | T1550 | |
phenodb:1122 | ABDOMEN: Liver > Structure > Steatosis > Microvesicular | HP:0001414 | ||
phenodb:1123 | ABDOMEN: Liver > Structure > Steatosis > Macrovesicular | HP:0001403 | ||
phenodb:3152 | ABDOMEN: Liver > Structure > Steatosis > Non-alcoholic | |||
phenodb:1124 | ABDOMEN: Liver > Structure > Steatosis > Other feature | |||
phenodb:1125 | ABDOMEN: Liver > Structure > Hepatomegaly | HP:0002240 | T1548 | |
phenodb:1126 | ABDOMEN: Liver > Structure > Intrahepatic cholestasis | HP:0001406 | T1542 | |
phenodb:1127 | ABDOMEN: Liver > Structure > Storage material in liver | |||
phenodb:1128 | ABDOMEN: Liver > Structure > Storage material in liver > Specify | |||
phenodb:2879 | ABDOMEN: Liver > Structure > Other feature | |||
phenodb:1129 | ABDOMEN: Liver > Function | |||
phenodb:1130 | ABDOMEN: Liver > Function > Cholestasis | HP:0001396 | T1541 | |
phenodb:1131 | ABDOMEN: Liver > Function > Dysfunction | HP:0001410 | T1544 | |
phenodb:1132 | ABDOMEN: Liver > Function > Failure | HP:0001399 | T1545 | |
phenodb:1133 | ABDOMEN: Liver > Function > Failure > Acute | HP:0006554 | T1546 | |
phenodb:1134 | ABDOMEN: Liver > Function > Failure > Chronic | HP:0100626 | T1547 | |
phenodb:1135 | ABDOMEN: Liver > Function > Failure > Other feature | |||
phenodb:1136 | ABDOMEN: Liver > Function > Jaundice | HP:0000952 | ||
phenodb:1137 | ABDOMEN: Liver > Function > Jaundice, neonatal | HP:0006579 | ||
phenodb:1138 | ABDOMEN: Liver > Function > Portal hypertension | HP:0001409 | T1552 | |
phenodb:2880 | ABDOMEN: Liver > Function > Other feature | |||
phenodb:3153 | ABDOMEN: Mesentery | HP:0100016 | T1454 | |
phenodb:3565 | ABDOMEN: Peritoneun | HP:0100768 | T2741 | |
phenodb:3165 | ABDOMEN: Peritoneun > Anomaly of the peritoneum | HP:0002585 | T1524 | |
phenodb:3166 | ABDOMEN: Peritoneun > Peritoneal abscess | HP:0100592 | T1523 | |
phenodb:1139 | ABDOMEN: Pancreas | HP:0001732 | ||
phenodb:1140 | ABDOMEN: Pancreas > Annular pancreas | HP:0001734 | T1556 | |
phenodb:3155 | ABDOMEN: Pancreas > Aplasia | HP:0100801 | ||
phenodb:3630 | ABDOMEN: Pancreas > Ectopic | HP:0006278 | T1558 | |
phenodb:1144 | ABDOMEN: Pancreas > Exocrine pancreatic insufficiency | HP:0001738 | T1561 | |
phenodb:3156 | ABDOMEN: Pancreas > Fistula | HP:0100844 | T1559 | |
phenodb:3154 | ABDOMEN: Pancreas > Hypoplastic | HP:0002594 | T1554 | |
phenodb:1145 | ABDOMEN: Pancreas > Islet cell hyperplasia | HP:0004510 | ||
phenodb:1146 | ABDOMEN: Pancreas > Islet cell hyperplasia > Diffuse | HP:0004510 | ||
phenodb:1147 | ABDOMEN: Pancreas > Islet cell hyperplasia > Nodular | |||
phenodb:1148 | ABDOMEN: Pancreas > Islet cell hyperplasia > Other feature | |||
phenodb:1141 | ABDOMEN: Pancreas > Pancreatic cysts | HP:0001737 | T1557 | |
phenodb:1142 | ABDOMEN: Pancreas > Pancreatic fibrosis | HP:0100732 | T1560 | |
phenodb:1143 | ABDOMEN: Pancreas > Pancreatitis | HP:0001733 | T1563 | |
phenodb:2881 | ABDOMEN: Pancreas > Other feature | |||
phenodb:1149 | ABDOMEN: Biliary tract | HP:0001080 | T1526 | |
phenodb:1150 | ABDOMEN: Biliary tract > Atresia | HP:0005912 | T6008 | |
phenodb:1152 | ABDOMEN: Biliary tract > Cholecystitis | HP:0001082 | T1538 | |
phenodb:1151 | ABDOMEN: Biliary tract > Cholelithiasis / Gallstones | HP:0001081 | T1536 | |
phenodb:1153 | ABDOMEN: Biliary tract > Gallbladder duplication | HP:0005608 | ||
phenodb:1154 | ABDOMEN: Biliary tract > Gallbladder, abnormal | HP:0005264 | T1528 | |
phenodb:3157 | ABDOMEN: Biliary tract > Gallbladder, absent | HP:0011467 | T1527 | |
phenodb:1155 | ABDOMEN: Biliary tract > Other feature | |||
phenodb:1156 | ABDOMEN: Spleen | HP:0001743 | ||
phenodb:1157 | ABDOMEN: Spleen > Accessory spleen | HP:0001747 | ||
phenodb:1158 | ABDOMEN: Spleen > Asplenia | HP:0001746 | T1566 | |
phenodb:3158 | ABDOMEN: Spleen > Hypersplenism | HP:0001971 | T1568 | |
phenodb:1160 | ABDOMEN: Spleen > Polysplenia | HP:0001748 | T1565 | |
phenodb:1159 | ABDOMEN: Spleen > Splenomegaly | HP:0001744 | T1567 | |
phenodb:1161 | ABDOMEN: Spleen > Other feature | |||
phenodb:1162 | GENITAL SYSTEM: | |||
phenodb:3159 | GENITAL SYSTEM: Ambiguous genitalia | HP:0000062 | T1946 | |
phenodb:3162 | GENITAL SYSTEM: Female pseudohermaphroditism | HP:0010458 | T1949 | |
phenodb:3164 | GENITAL SYSTEM: Gonadal dysgenesis | HP:0000133 | T1951 | |
phenodb:3161 | GENITAL SYSTEM: Male pseudohermaphroditism | HP:0000037 | T1948 | |
phenodb:3163 | GENITAL SYSTEM: Maternal virilization in pregnancy | HP:0008072 | T1950 | |
phenodb:3160 | GENITAL SYSTEM: True hermaphroditism | HP:0010459 | T1947 | |
phenodb:3168 | GENITAL SYSTEM: Urogenital fistula | HP:0100589 | T1888 | |
phenodb:3167 | GENITAL SYSTEM: Urogenital sinus anomaly | HP:0100779 | T1979 | |
phenodb:1163 | GENITAL SYSTEM: Male | HP:0010461 | ||
phenodb:1164 | GENITAL SYSTEM: Male > Structure | HP:0000022 | T2017 | |
phenodb:1165 | GENITAL SYSTEM: Male > Structure > Penis / Phallus | HP:0000036 | T1980 | |
phenodb:3169 | GENITAL SYSTEM: Male > Structure > Penis / Phallus > Bifid penis (aka diphallia) | HP:0100599 | T1993 | |
phenodb:1166 | GENITAL SYSTEM: Male > Structure > Penis / Phallus > Chordee | HP:0000041 | T1985 | |
phenodb:3170 | GENITAL SYSTEM: Male > Structure > Penis / Phallus > Epispadias | HP:0000039 | T1984 | |
phenodb:1167 | GENITAL SYSTEM: Male > Structure > Penis / Phallus > Freckles on penis | |||
phenodb:1168 | GENITAL SYSTEM: Male > Structure > Penis / Phallus > Hypospadias | HP:0000047 | T1983 | |
phenodb:1169 | GENITAL SYSTEM: Male > Structure > Penis / Phallus > Hypospadias > Glandular | HP:0000807 | T1989 | |
phenodb:1170 | GENITAL SYSTEM: Male > Structure > Penis / Phallus > Hypospadias > Subcoronal | HP:0008743 | T1987 | |
phenodb:1171 | GENITAL SYSTEM: Male > Structure > Penis / Phallus > Hypospadias > Midshaft | HP:0012854 | ||
phenodb:1172 | GENITAL SYSTEM: Male > Structure > Penis / Phallus > Hypospadias > Penoscrotal | HP:0000808 | T1988 | |
phenodb:1173 | GENITAL SYSTEM: Male > Structure > Penis / Phallus > Hypospadias > Scrotal | HP:0012853 | ||
phenodb:1174 | GENITAL SYSTEM: Male > Structure > Penis / Phallus > Hypospadias > Perineal | HP:0000051 | T1986 | |
phenodb:1175 | GENITAL SYSTEM: Male > Structure > Penis / Phallus > Hypospadias > Other feature | |||
phenodb:1176 | GENITAL SYSTEM: Male > Structure > Penis / Phallus > Macropenis (aka Large penis) | HP:0000040 | T1982 | |
phenodb:1177 | GENITAL SYSTEM: Male > Structure > Penis / Phallus > Micropenis (aka Small penis) | HP:0000054 | T1981 | |
phenodb:3171 | GENITAL SYSTEM: Male > Structure > Penis / Phallus > Paraphimosis | HP:0100588 | T1992 | |
phenodb:1178 | GENITAL SYSTEM: Male > Structure > Penis / Phallus > Penoscrotal inversion | HP:0100600 | T1994 | |
phenodb:1179 | GENITAL SYSTEM: Male > Structure > Penis / Phallus > Phimosis | HP:0001741 | ||
phenodb:3172 | GENITAL SYSTEM: Male > Structure > Penis / Phallus > Sclerosis of the corpus cavernosum | HP:0100624 | T1990 | |
phenodb:2882 | GENITAL SYSTEM: Male > Structure > Penis / Phallus > Other feature | |||
phenodb:1180 | GENITAL SYSTEM: Male > Structure > Scrotum | HP:0000045 | ||
phenodb:1181 | GENITAL SYSTEM: Male > Structure > Scrotum > Bifid scrotum | HP:0000048 | T2011 | |
phenodb:1182 | GENITAL SYSTEM: Male > Structure > Scrotum > Hyperpigmented | HP:0012855 | ||
phenodb:1183 | GENITAL SYSTEM: Male > Structure > Scrotum > Median raphe prominent | HP:0003246 | ||
phenodb:1184 | GENITAL SYSTEM: Male > Structure > Scrotum > Rugation | HP:0012856 | ||
phenodb:1185 | GENITAL SYSTEM: Male > Structure > Scrotum > Rugation > Under-rugated | HP:0012858 | ||
phenodb:1186 | GENITAL SYSTEM: Male > Structure > Scrotum > Rugation > Over-rugated | HP:0012857 | ||
phenodb:1187 | GENITAL SYSTEM: Male > Structure > Scrotum > Rugation > Other feature | |||
phenodb:1188 | GENITAL SYSTEM: Male > Structure > Scrotum > Shawl scrotum | HP:0000049 | T2010 | |
phenodb:3173 | GENITAL SYSTEM: Male > Structure > Scrotum > Small | HP:0000046 | T2009 | |
phenodb:2883 | GENITAL SYSTEM: Male > Structure > Scrotum > Other feature | |||
phenodb:1189 | GENITAL SYSTEM: Male > Structure > Testes | HP:0000035 | T1995 | |
phenodb:3174 | GENITAL SYSTEM: Male > Structure > Testes > Absent | HP:0010469 | T1998 | |
phenodb:3175 | GENITAL SYSTEM: Male > Structure > Testes > Atrophic | HP:0000029 | T2004 | |
phenodb:1190 | GENITAL SYSTEM: Male > Structure > Testes > Cryptorchidism (aka Undescended testes) | HP:0000028 | ||
phenodb:1191 | GENITAL SYSTEM: Male > Structure > Testes > Cryptorchidism (aka Undescended testes) > Unilateral | HP:0012741 | T2001 | |
phenodb:1192 | GENITAL SYSTEM: Male > Structure > Testes > Cryptorchidism (aka Undescended testes) > Bilateral | HP:0008689 | T2002 | |
phenodb:3179 | GENITAL SYSTEM: Male > Structure > Testes > Dysgenetic | HP:0008715 | T2005 | |
phenodb:1193 | GENITAL SYSTEM: Male > Structure > Testes > Epididymitis | HP:0000031 | ||
phenodb:1194 | GENITAL SYSTEM: Male > Structure > Testes > Fibrotic testes | HP:0012860 | T1996 | |
phenodb:1195 | GENITAL SYSTEM: Male > Structure > Testes > Gonadoblastoma | HP:0000150 | ||
phenodb:1196 | GENITAL SYSTEM: Male > Structure > Testes > Hydrocele | HP:0000034 | T2012 | |
phenodb:3176 | GENITAL SYSTEM: Male > Structure > Testes > Hyperplastic Leydig cells | HP:0010791 | T1999 | |
phenodb:1197 | GENITAL SYSTEM: Male > Structure > Testes > Inguinal hernia | HP:0000023 | T0886 | |
phenodb:1198 | GENITAL SYSTEM: Male > Structure > Testes > Macroorchidism (aka Large testes) | HP:0000053 | T2006 | |
phenodb:3177 | GENITAL SYSTEM: Male > Structure > Testes > Orchitis | HP:0100796 | T2018 | |
phenodb:1199 | GENITAL SYSTEM: Male > Structure > Testes > Ovotestes | HP:0012861 | ||
phenodb:1200 | GENITAL SYSTEM: Male > Structure > Testes > Prostatitis | HP:0000024 | T1934 | |
phenodb:1201 | GENITAL SYSTEM: Male > Structure > Testes > Small / Hypoplastic testes | HP:0008734 | T2003 | |
phenodb:1202 | GENITAL SYSTEM: Male > Structure > Testes > Sperm | HP:0012864 | ||
phenodb:1203 | GENITAL SYSTEM: Male > Structure > Testes > Sperm > Azoospermia | HP:0000027 | T2029 | |
phenodb:1204 | GENITAL SYSTEM: Male > Structure > Testes > Sperm > Head defects | HP:0012865 | ||
phenodb:1205 | GENITAL SYSTEM: Male > Structure > Testes > Sperm > Midpiece defects | HP:0012867 | ||
phenodb:1206 | GENITAL SYSTEM: Male > Structure > Testes > Sperm > Motility abnormal | HP:0012206 | ||
phenodb:3181 | GENITAL SYSTEM: Male > Structure > Testes > Sperm > Oligospermia | HP:0000798 | T2028 | |
phenodb:1207 | GENITAL SYSTEM: Male > Structure > Testes > Sperm > Tail defects | HP:0012868 | ||
phenodb:1208 | GENITAL SYSTEM: Male > Structure > Testes > Sperm > Other feature | |||
phenodb:3178 | GENITAL SYSTEM: Male > Structure > Testes > Supernumerary testes | HP:0010470 | T1997 | |
phenodb:3180 | GENITAL SYSTEM: Male > Structure > Testes > Torsion | HP:0100813 | T2007 | |
phenodb:1209 | GENITAL SYSTEM: Male > Structure > Testes > Vanishing testes | HP:0012870 | ||
phenodb:1210 | GENITAL SYSTEM: Male > Structure > Testes > Vanishing testes > Unilateral | |||
phenodb:1211 | GENITAL SYSTEM: Male > Structure > Testes > Vanishing testes > Bilateral | |||
phenodb:1212 | GENITAL SYSTEM: Male > Structure > Testes > Varicocele | HP:0012871 | ||
phenodb:1213 | GENITAL SYSTEM: Male > Structure > Testes > Vas deferens, congenital absence | HP:0012873 | ||
phenodb:1214 | GENITAL SYSTEM: Male > Structure > Testes > Vas deferens, congenital absence > Unilateral | |||
phenodb:1215 | GENITAL SYSTEM: Male > Structure > Testes > Vas deferens, congenital absence > Bilateral | |||
phenodb:2884 | GENITAL SYSTEM: Male > Structure > Testes > Other feature | |||
phenodb:1216 | GENITAL SYSTEM: Male > Function | |||
phenodb:1217 | GENITAL SYSTEM: Male > Function > Erectile dysfunction | HP:0000802 | T2034 | |
phenodb:1218 | GENITAL SYSTEM: Male > Function > Ejaculatory incompetence | HP:0012879 | ||
phenodb:1219 | GENITAL SYSTEM: Male > Function > Infertility | HP:0003251 | T2025 | |
phenodb:1220 | GENITAL SYSTEM: Male > Function > Premature ejaculation | HP:0012876 | ||
phenodb:3182 | GENITAL SYSTEM: Male > Function > Priapism | HP:0200023 | T2030 | |
phenodb:1221 | GENITAL SYSTEM: Male > Function > Retrograde ejaculation | HP:0012877 | ||
phenodb:1222 | GENITAL SYSTEM: Male > Function > Other feature | |||
phenodb:1223 | GENITAL SYSTEM: Female | HP:0010460 | ||
phenodb:1224 | GENITAL SYSTEM: Female > Structure | |||
phenodb:1225 | GENITAL SYSTEM: Female > Structure > Clitoris | HP:0000056 | ||
phenodb:1226 | GENITAL SYSTEM: Female > Structure > Clitoris > Clitoromegaly | HP:0000057 | T1956 | |
phenodb:1227 | GENITAL SYSTEM: Female > Structure > Clitoris > Small | HP:0000060 | T1958 | |
phenodb:2885 | GENITAL SYSTEM: Female > Structure > Clitoris > Other feature | |||
phenodb:2919 | GENITAL SYSTEM: Female > Structure > Labia | HP:0000058 | T1961 | |
phenodb:1228 | GENITAL SYSTEM: Female > Structure > Labia > Labia, fused | HP:0000063 | T1955 | |
phenodb:1229 | GENITAL SYSTEM: Female > Structure > Labia > Labia minora | HP:0012880 | ||
phenodb:1230 | GENITAL SYSTEM: Female > Structure > Labia > Labia minora > Hyperplastic | HP:0008694 | T1962 | |
phenodb:1231 | GENITAL SYSTEM: Female > Structure > Labia > Labia minora > Hypoplastic | HP:0000064 | ||
phenodb:1232 | GENITAL SYSTEM: Female > Structure > Labia > Labia minora > Other feature | |||
phenodb:1233 | GENITAL SYSTEM: Female > Structure > Labia > Labia majora | HP:0012881 | ||
phenodb:1234 | GENITAL SYSTEM: Female > Structure > Labia > Labia majora > Hyperplastic | HP:0012882 | T1960 | |
phenodb:1235 | GENITAL SYSTEM: Female > Structure > Labia > Labia majora > Hypoplastic | HP:0000059 | T1954 | |
phenodb:1236 | GENITAL SYSTEM: Female > Structure > Labia > Labia majora > Other feature | |||
phenodb:2920 | GENITAL SYSTEM: Female > Structure > Labia > Other feature | |||
phenodb:1237 | GENITAL SYSTEM: Female > Structure > Ovaries | HP:0000137 | T1975 | |
phenodb:1241 | GENITAL SYSTEM: Female > Structure > Ovaries > Gonadoblastoma | HP:0000150 | ||
phenodb:1242 | GENITAL SYSTEM: Female > Structure > Ovaries > Absent | HP:0010463 | T1978 | |
phenodb:1243 | GENITAL SYSTEM: Female > Structure > Ovaries > Absent > Unilateral | |||
phenodb:1244 | GENITAL SYSTEM: Female > Structure > Ovaries > Absent > Bilateral | |||
phenodb:1245 | GENITAL SYSTEM: Female > Structure > Ovaries > Cysts | HP:0000138 | ||
phenodb:1246 | GENITAL SYSTEM: Female > Structure > Ovaries > Cysts > Hemorrhagic | HP:0012886 | ||
phenodb:1247 | GENITAL SYSTEM: Female > Structure > Ovaries > Cysts > Serous | HP:0012887 | ||
phenodb:1248 | GENITAL SYSTEM: Female > Structure > Ovaries > Polycystic | HP:0000147 | T1976 | |
phenodb:1249 | GENITAL SYSTEM: Female > Structure > Ovaries > Streak | HP:0010464 | T1977 | |
phenodb:2922 | GENITAL SYSTEM: Female > Structure > Ovaries > Other feature | |||
phenodb:2921 | GENITAL SYSTEM: Female > Structure > Fallopian tubes | HP:0008655 | ||
phenodb:1238 | GENITAL SYSTEM: Female > Structure > Fallopian tubes > Absent | HP:0008655 | ||
phenodb:1239 | GENITAL SYSTEM: Female > Structure > Fallopian tubes > Cysts | HP:0012883 | ||
phenodb:1240 | GENITAL SYSTEM: Female > Structure > Fallopian tubes > Duplicated | HP:0012885 | ||
phenodb:2886 | GENITAL SYSTEM: Female > Structure > Fallopian tubes > Other feature | |||
phenodb:1250 | GENITAL SYSTEM: Female > Structure > Uterus | HP:0000130 | T1963 | |
phenodb:1251 | GENITAL SYSTEM: Female > Structure > Uterus > Cervix, absent | |||
phenodb:1252 | GENITAL SYSTEM: Female > Structure > Uterus > Cervix, incompetent | HP:0030009 | ||
phenodb:1255 | GENITAL SYSTEM: Female > Structure > Uterus > Mullerian duct derivative dysgenesis | |||
phenodb:1257 | GENITAL SYSTEM: Female > Structure > Uterus > Absent | HP:0000151 | T1964 | |
phenodb:1258 | GENITAL SYSTEM: Female > Structure > Uterus > Bicornuate | HP:0000813 | T1965 | |
phenodb:1259 | GENITAL SYSTEM: Female > Structure > Uterus > Fibroids | HP:0000131 | ||
phenodb:1260 | GENITAL SYSTEM: Female > Structure > Uterus > Prolapse | HP:0000139 | T1966 | |
phenodb:3183 | GENITAL SYSTEM: Female > Structure > Uterus > Rupture | HP:0100718 | T2019 | |
phenodb:1264 | GENITAL SYSTEM: Female > Structure > Uterus > Other feature | |||
phenodb:2923 | GENITAL SYSTEM: Female > Structure > Vagina | HP:0000142 | T1969 | |
phenodb:1253 | GENITAL SYSTEM: Female > Structure > Vagina > Hydrometrocolpos | HP:0030010 | ||
phenodb:1254 | GENITAL SYSTEM: Female > Structure > Vagina > Imperforate hymen | HP:0030011 | ||
phenodb:1256 | GENITAL SYSTEM: Female > Structure > Vagina > Rectovaginal fistula | HP:0000143 | T1479 | |
phenodb:1261 | GENITAL SYSTEM: Female > Structure > Vagina > Atresia | HP:0000148 | T1970 | |
phenodb:1262 | GENITAL SYSTEM: Female > Structure > Vagina > Septate | HP:0001153 | T1971 | |
phenodb:3184 | GENITAL SYSTEM: Female > Structure > Vagina > Short | HP:0008726 | T1972 | |
phenodb:1263 | GENITAL SYSTEM: Female > Structure > Vagina > Vesicovaginal fistula | HP:0001586 | T1878 | |
phenodb:2924 | GENITAL SYSTEM: Female > Structure > Vagina > Other feature | |||
phenodb:1265 | GENITAL SYSTEM: Female > Function | |||
phenodb:1266 | GENITAL SYSTEM: Female > Function > Amenorrhea, primary | HP:0000786 | T2092 | |
phenodb:1267 | GENITAL SYSTEM: Female > Function > Amenorrhea, secondary | HP:0000869 | ||
phenodb:3185 | GENITAL SYSTEM: Female > Function > Dysmenorrhea | HP:0100607 | T2022 | |
phenodb:1268 | GENITAL SYSTEM: Female > Function > Endometriosis | HP:0030127 | ||
phenodb:1269 | GENITAL SYSTEM: Female > Function > Infertility | HP:0008222 | T2026 | |
phenodb:1270 | GENITAL SYSTEM: Female > Function > Menorrhagia | HP:0000132 | T2021 | |
phenodb:1271 | GENITAL SYSTEM: Female > Function > Menstrual periods, irregular | HP:0000858 | T2091 | |
phenodb:3186 | GENITAL SYSTEM: Female > Function > Metrorrhagia | HP:0100608 | T2023 | |
phenodb:1272 | GENITAL SYSTEM: Female > Function > Sexual | HP:0030014 | ||
phenodb:1273 | GENITAL SYSTEM: Female > Function > Sexual > Anorgasmia | HP:0030015 | ||
phenodb:1274 | GENITAL SYSTEM: Female > Function > Sexual > Dyspareunia | HP:0030016 | ||
phenodb:1275 | GENITAL SYSTEM: Female > Function > Sexual > Libido diminished | HP:0030018 | ||
phenodb:1276 | GENITAL SYSTEM: Female > Function > Sexual > Libido increased | HP:0030019 | ||
phenodb:1277 | GENITAL SYSTEM: Female > Function > Sexual > Other feature | |||
phenodb:2887 | GENITAL SYSTEM: Female > Function > Other feature | |||
phenodb:1278 | URINARY SYSTEM: | HP:0000079 | ||
phenodb:1279 | URINARY SYSTEM: Kidneys | HP:0000077 | T1852 | |
phenodb:1280 | URINARY SYSTEM: Kidneys > Structure | |||
phenodb:3187 | URINARY SYSTEM: Kidneys > Structure > Atrophy | HP:0012585 | T1855 | |
phenodb:1281 | URINARY SYSTEM: Kidneys > Structure > Corticomedullary cysts | HP:0000108 | T1857 | |
phenodb:1282 | URINARY SYSTEM: Kidneys > Structure > Diffuse lamellation of the glomerular basement membrane | HP:0030034 | ||
phenodb:1283 | URINARY SYSTEM: Kidneys > Structure > Focal segmental glomerulosclerosis | HP:0000097 | T1905 | |
phenodb:1284 | URINARY SYSTEM: Kidneys > Structure > Glomerulonephritis | HP:0000099 | T1906 | |
phenodb:1285 | URINARY SYSTEM: Kidneys > Structure > Glomerulosclerosis | HP:0000096 | T1907 | |
phenodb:1286 | URINARY SYSTEM: Kidneys > Structure > Horseshoe kidney | HP:0000085 | T1863 | |
phenodb:1287 | URINARY SYSTEM: Kidneys > Structure > Hydronephrosis | HP:0000126 | T1891 | |
phenodb:1288 | URINARY SYSTEM: Kidneys > Structure > Interstitial fibrosis | HP:0005576 | ||
phenodb:1289 | URINARY SYSTEM: Kidneys > Structure > Kidneys, absent / Renal agenesis | HP:0000104 | ||
phenodb:1290 | URINARY SYSTEM: Kidneys > Structure > Kidneys, absent / Renal agenesis > Unilateral | HP:0000122 | ||
phenodb:1291 | URINARY SYSTEM: Kidneys > Structure > Kidneys, absent / Renal agenesis > Bilateral | HP:0010958 | T1860 | |
phenodb:1292 | URINARY SYSTEM: Kidneys > Structure > Kidneys, ectopic | HP:0000086 | T1864 | |
phenodb:1293 | URINARY SYSTEM: Kidneys > Structure > Kidneys, hypoplastic | HP:0000089 | T1854 | |
phenodb:1294 | URINARY SYSTEM: Kidneys > Structure > Kidneys, hypoplastic > Unilateral | HP:0012583 | ||
phenodb:1295 | URINARY SYSTEM: Kidneys > Structure > Kidneys, hypoplastic > Bilateral | HP:0012584 | ||
phenodb:3189 | URINARY SYSTEM: Kidneys > Structure > Kidneys, large | HP:0000105 | T1858 | |
phenodb:1296 | URINARY SYSTEM: Kidneys > Structure > Kidneys, multicystic dysplastic | HP:0000003 | T1869 | |
phenodb:1297 | URINARY SYSTEM: Kidneys > Structure > Mesangial sclerosis | HP:0001967 | ||
phenodb:1298 | URINARY SYSTEM: Kidneys > Structure > Nephritis | HP:0000123 | ||
phenodb:1299 | URINARY SYSTEM: Kidneys > Structure > Nephrocalcinosis | HP:0000121 | T1920 | |
phenodb:1300 | URINARY SYSTEM: Kidneys > Structure > Nephrolithiasis | HP:0000787 | T1922 | |
phenodb:1301 | URINARY SYSTEM: Kidneys > Structure > Nephrolithiasis > Calcium | HP:0004724 | ||
phenodb:1302 | URINARY SYSTEM: Kidneys > Structure > Nephrolithiasis > Oxalate | HP:0008672 | ||
phenodb:1303 | URINARY SYSTEM: Kidneys > Structure > Nephrolithiasis > Struvite | HP:0030035 | ||
phenodb:1304 | URINARY SYSTEM: Kidneys > Structure > Nephrolithiasis > Uric acid | HP:0000791 | ||
phenodb:1305 | URINARY SYSTEM: Kidneys > Structure > Nephrolithiasis > Other feature | |||
phenodb:1306 | URINARY SYSTEM: Kidneys > Structure > Nephronophthisis | HP:0000090 | T1856 | |
phenodb:1307 | URINARY SYSTEM: Kidneys > Structure > Pelvic kidney | HP:0000125 | T1865 | |
phenodb:1308 | URINARY SYSTEM: Kidneys > Structure > Polycystic kidneys | HP:0000113 | T1870 | |
phenodb:3188 | URINARY SYSTEM: Kidneys > Structure > Renal pelvis duplication | HP:0005580 | T1880 | |
phenodb:3190 | URINARY SYSTEM: Kidneys > Structure > Renal tubular dysgenesis | HP:0008660 | T1917 | |
phenodb:3191 | URINARY SYSTEM: Kidneys > Structure > Single renal cyst | HP:0012581 | T1871 | |
phenodb:3192 | URINARY SYSTEM: Kidneys > Structure > Supernumerary kidneys | HP:0000075 | T1866 | |
phenodb:3193 | URINARY SYSTEM: Kidneys > Structure > Tubulointerstitial nephritis | HP:0001970 | T1916 | |
phenodb:1309 | URINARY SYSTEM: Kidneys > Structure > Other feature | |||
phenodb:1310 | URINARY SYSTEM: Kidneys > Function | |||
phenodb:3197 | URINARY SYSTEM: Kidneys > Function > Anuria | HP:0100519 | T1939 | |
phenodb:1311 | URINARY SYSTEM: Kidneys > Function > End stage renal disease / Renal failure | HP:0003774 | T1919 | |
phenodb:1312 | URINARY SYSTEM: Kidneys > Function > Glomerulonephropathy | HP:0100820 | T1904 | |
phenodb:1313 | URINARY SYSTEM: Kidneys > Function > Hematuria | HP:0000790 | T1932 | |
phenodb:1314 | URINARY SYSTEM: Kidneys > Function > Hyperreninemia | HP:0000848 | ||
phenodb:1315 | URINARY SYSTEM: Kidneys > Function > Isosthenuria (inability to concentrate urine) | HP:0030036 | ||
phenodb:3194 | URINARY SYSTEM: Kidneys > Function > Microscopic hematuria | HP:0002907 | T1931 | |
phenodb:1316 | URINARY SYSTEM: Kidneys > Function > Myoglobinuria | HP:0002913 | ||
phenodb:3195 | URINARY SYSTEM: Kidneys > Function > Nephrogenic diabetes insipidus | HP:0009806 | T2051 | |
phenodb:1317 | URINARY SYSTEM: Kidneys > Function > Nephrotic syndrome | HP:0000100 | T1929 | |
phenodb:3196 | URINARY SYSTEM: Kidneys > Function > Oliguria | HP:0100520 | T1937 | |
phenodb:1318 | URINARY SYSTEM: Kidneys > Function > Polyuria | HP:0000103 | ||
phenodb:1319 | URINARY SYSTEM: Kidneys > Function > Proteinuria | HP:0000093 | T1930 | |
phenodb:1321 | URINARY SYSTEM: Kidneys > Function > Proximal renal tubule defect | HP:0000114 | ||
phenodb:1320 | URINARY SYSTEM: Kidneys > Function > Pyelonephritis | HP:0012330 | ||
phenodb:1324 | URINARY SYSTEM: Kidneys > Function > Renal calcium wasting | HP:0002150 | ||
phenodb:1322 | URINARY SYSTEM: Kidneys > Function > Renal Fanconi syndrome | HP:0001994 | T1913 | |
phenodb:1323 | URINARY SYSTEM: Kidneys > Function > Renal insufficiency | HP:0000083 | T1901 | |
phenodb:1325 | URINARY SYSTEM: Kidneys > Function > Renal magnesium wasting | HP:0005567 | ||
phenodb:1326 | URINARY SYSTEM: Kidneys > Function > Renal phosphate wasting | HP:0000117 | T1912 | |
phenodb:1327 | URINARY SYSTEM: Kidneys > Function > Renal potassium wasting | HP:0000128 | T1911 | |
phenodb:1328 | URINARY SYSTEM: Kidneys > Function > Renal sodium wasting | HP:0012606 | T1903 | |
phenodb:1329 | URINARY SYSTEM: Kidneys > Function > Tubular acidosis | HP:0001947 | T1910 | |
phenodb:3198 | URINARY SYSTEM: Kidneys > Function > Tubular dysfunction | HP:0000124 | T1908 | |
phenodb:1331 | URINARY SYSTEM: Kidneys > Function > Tubulopathy, distal | |||
phenodb:1330 | URINARY SYSTEM: Kidneys > Function > Tubulopathy, proximal | HP:0000114 | T1914 | |
phenodb:1332 | URINARY SYSTEM: Kidneys > Function > Other feature | |||
phenodb:1333 | URINARY SYSTEM: Ureters | HP:0000069 | T1881 | |
phenodb:1334 | URINARY SYSTEM: Ureters > Bifid ureter | HP:0030037 | ||
phenodb:1335 | URINARY SYSTEM: Ureters > Hydroureter | HP:0000072 | ||
phenodb:1336 | URINARY SYSTEM: Ureters > Megaureter | HP:0008676 | T1892 | |
phenodb:1337 | URINARY SYSTEM: Ureters > Ureteral duplication | HP:0000073 | T1879 | |
phenodb:1338 | URINARY SYSTEM: Ureters > Ureteral stenosis | HP:0000071 | T1890 | |
phenodb:1339 | URINARY SYSTEM: Ureters > Ureterocele | HP:0000070 | T1883 | |
phenodb:1340 | URINARY SYSTEM: Ureters > Ureteropelvic junction obstruction | HP:0000074 | T1893 | |
phenodb:3199 | URINARY SYSTEM: Ureters > Ureterovesical stenosis | HP:0008714 | T1882 | |
phenodb:1341 | URINARY SYSTEM: Ureters > Vesicoureteral reflux | HP:0000076 | T1899 | |
phenodb:1342 | URINARY SYSTEM: Ureters > Other feature | |||
phenodb:1343 | URINARY SYSTEM: Bladder | HP:0000014 | T1874 | |
phenodb:3200 | URINARY SYSTEM: Bladder > Absent/agenesis | HP:0010477 | T1876 | |
phenodb:3201 | URINARY SYSTEM: Bladder > Cystocele | HP:0100645 | T1889 | |
phenodb:3202 | URINARY SYSTEM: Bladder > Distended | HP:0010955 | T1877 | |
phenodb:1344 | URINARY SYSTEM: Bladder > Diverticula | HP:0000015 | T1887 | |
phenodb:3203 | URINARY SYSTEM: Bladder > Dysuria | HP:0100518 | T1940 | |
phenodb:1345 | URINARY SYSTEM: Bladder > Enuresis | HP:0000805 | ||
phenodb:1346 | URINARY SYSTEM: Bladder > Exstrophy | HP:0002836 | T1885 | |
phenodb:3204 | URINARY SYSTEM: Bladder > Fistula | HP:0004321 | T1875 | |
phenodb:1347 | URINARY SYSTEM: Bladder > Infections, recurrent | HP:0000010 | T1933 | |
phenodb:1348 | URINARY SYSTEM: Bladder > Neurogenic bladder | HP:0000011 | ||
phenodb:3205 | URINARY SYSTEM: Bladder > Pollakisuria | HP:0100515 | ||
phenodb:1349 | URINARY SYSTEM: Bladder > Sphincter disturbances | HP:0002839 | ||
phenodb:1350 | URINARY SYSTEM: Bladder > Urinary hesitancy | HP:0000019 | T1942 | |
phenodb:1351 | URINARY SYSTEM: Bladder > Urinary incontinence | HP:0000020 | ||
phenodb:1352 | URINARY SYSTEM: Bladder > Urinary urgency | HP:0000012 | ||
phenodb:1353 | URINARY SYSTEM: Bladder > Other feature | |||
phenodb:3206 | URINARY SYSTEM: Urethra | HP:0000795 | T1894 | |
phenodb:3209 | URINARY SYSTEM: Urethra > Diverticulum | HP:0008722 | T1897 | |
phenodb:3210 | URINARY SYSTEM: Urethra > Fistula | HP:0010480 | T1898 | |
phenodb:3207 | URINARY SYSTEM: Urethra > Posterior urethral valves | HP:0010957 | T1895 | |
phenodb:3208 | URINARY SYSTEM: Urethra > Stenosis | HP:0008661 | T1896 | |
phenodb:3211 | URINARY SYSTEM: Urethra > Other feature | |||
phenodb:1354 | SKELETAL: | HP:0000924 | ||
phenodb:1355 | SKELETAL: General | |||
phenodb:1356 | SKELETAL: General > Bone age | HP:0000927 | ||
phenodb:1357 | SKELETAL: General > Bone age > Advanced | HP:0005616 | T2451 | |
phenodb:1358 | SKELETAL: General > Bone age > Delayed | HP:0002750 | T2450 | |
phenodb:1359 | SKELETAL: General > Bone age > Other feature | |||
phenodb:3212 | SKELETAL: General > Bone cyst | HP:0012062 | T2457 | |
phenodb:1360 | SKELETAL: General > Contractures | HP:0001371 | ||
phenodb:3671 | SKELETAL: General > Demineralization of Bone | HP:0004349 | T2431 | |
phenodb:1361 | SKELETAL: General > Density | HP:0004348 | ||
phenodb:1362 | SKELETAL: General > Density > Increased | HP:0011001 | ||
phenodb:1363 | SKELETAL: General > Density > Decreased | HP:0006462 | ||
phenodb:1364 | SKELETAL: General > Density > Other feature | |||
phenodb:1365 | SKELETAL: General > Dysplasias | HP:0002652 | T2437 | |
phenodb:1366 | SKELETAL: General > Dysplasias > Multiple epiphyseal dysplasia | HP:0002654 | ||
phenodb:1367 | SKELETAL: General > Dysplasias > Spondylo- (spine) dysplasia | |||
phenodb:1368 | SKELETAL: General > Dysplasias > Spondyloepiphyseal dysplasia | HP:0002655 | ||
phenodb:1369 | SKELETAL: General > Dysplasias > Spondyloepimetaphyseal dysplasia | HP:0002651 | ||
phenodb:1370 | SKELETAL: General > Dysplasias > Spondylometaphyseal dysplasia | HP:0002657 | ||
phenodb:1371 | SKELETAL: General > Dysplasias > Other feature | |||
phenodb:1372 | SKELETAL: General > Epiphyseal abnormalities, generalized | HP:0005930 | T2468 | |
phenodb:1373 | SKELETAL: General > Epiphyseal abnormalities, generalized > Cone-shaped | HP:0010579 | T2477 | |
phenodb:1374 | SKELETAL: General > Epiphyseal abnormalities, generalized > Delayed ossification | HP:0003947 | ||
phenodb:1375 | SKELETAL: General > Epiphyseal abnormalities, generalized > Dysplasia | HP:0002656 | T2469 | |
phenodb:1376 | SKELETAL: General > Epiphyseal abnormalities, generalized > Enlarged | HP:0010580 | T2474 | |
phenodb:1377 | SKELETAL: General > Epiphyseal abnormalities, generalized > Irregular | HP:0010582 | T2473 | |
phenodb:3213 | SKELETAL: General > Epiphyseal abnormalities, generalized > Ivory epiphysis | HP:0010583 | T2472 | |
phenodb:1378 | SKELETAL: General > Epiphyseal abnormalities, generalized > Small | HP:0010585 | T2471 | |
phenodb:1379 | SKELETAL: General > Epiphyseal abnormalities, generalized > Stippled / Punctate | HP:0010655 | T2470 | |
phenodb:1380 | SKELETAL: General > Epiphyseal abnormalities, generalized > Other feature | |||
phenodb:1381 | SKELETAL: General > Metaphyseal abnormalities, generalized | HP:0000944 | ||
phenodb:1382 | SKELETAL: General > Metaphyseal abnormalities, generalized > Cupping | HP:0003021 | T2467 | |
phenodb:1383 | SKELETAL: General > Metaphyseal abnormalities, generalized > Dysplasia | HP:0100255 | T2463 | |
phenodb:1384 | SKELETAL: General > Metaphyseal abnormalities, generalized > Frayed, irregular | HP:0003025 | T2465 | |
phenodb:1385 | SKELETAL: General > Metaphyseal abnormalities, generalized > Flared | HP:0003015 | T2466 | |
phenodb:1386 | SKELETAL: General > Metaphyseal abnormalities, generalized > Widened | HP:0003016 | T2464 | |
phenodb:1387 | SKELETAL: General > Metaphyseal abnormalities, generalized > Other feature | |||
phenodb:3214 | SKELETAL: General > Diaphyseal anomaly | HP:0100252 | T2480 | |
phenodb:3215 | SKELETAL: General > Diaphyseal anomaly > Narrow | HP:0003100 | T2483 | |
phenodb:3216 | SKELETAL: General > Diaphyseal anomaly > Other feature | |||
phenodb:1388 | SKELETAL: General > Dysostosis multiplex | HP:0000943 | ||
phenodb:1389 | SKELETAL: General > Enchondromas | HP:0030038 | ||
phenodb:1390 | SKELETAL: General > Exostoses | HP:0100777 | T2445 | |
phenodb:1391 | SKELETAL: General > Fractures, diffuse | HP:0002757 | T2442 | |
phenodb:1392 | SKELETAL: General > Fragility | HP:0002659 | T2443 | |
phenodb:3217 | SKELETAL: General > Hyperostosis | HP:0100774 | T2435 | |
phenodb:1393 | SKELETAL: General > Joints, generalized | HP:0001367 | T2486 | |
phenodb:1394 | SKELETAL: General > Joints, generalized > Dislocation(s) | HP:0001373 | T2505 | |
phenodb:1395 | SKELETAL: General > Joints, generalized > Enlarged | HP:0003037 | ||
phenodb:1396 | SKELETAL: General > Joints, generalized > Fused | |||
phenodb:1397 | SKELETAL: General > Joints, generalized > Hemarthrosis | HP:0005261 | T2604 | |
phenodb:3219 | SKELETAL: General > Joints, generalized > Intraarticular calcification | |||
phenodb:1398 | SKELETAL: General > Joints, generalized > Laxity | HP:0001388 | T2499 | |
phenodb:3220 | SKELETAL: General > Joints, generalized > Laxity > Hyperlaxity of small joints | |||
phenodb:3221 | SKELETAL: General > Joints, generalized > Laxity > Hyperlaxity of large joints | |||
phenodb:1399 | SKELETAL: General > Joints, generalized > Stiff | HP:0001387 | T2492 | |
phenodb:3222 | SKELETAL: General > Joints, generalized > Subluxation | |||
phenodb:3223 | SKELETAL: General > Joints, generalized > Synostosis | HP:0100240 | T2436 | |
phenodb:1400 | SKELETAL: General > Joints, generalized > Other feature | |||
phenodb:1401 | SKELETAL: General > Osteoarthritis | HP:0002758 | ||
phenodb:3224 | SKELETAL: General > Osteochondrosis | HP:0040188 | T2438 | |
phenodb:3225 | SKELETAL: General > Osteochondritis | |||
phenodb:3226 | SKELETAL: General > Osteomyelitis | HP:0002754 | T2460 | |
phenodb:3227 | SKELETAL: General > Osteolysis | HP:0002797 | T2453 | |
phenodb:1402 | SKELETAL: General > Osteomalacia | HP:0002749 | T2430 | |
phenodb:1403 | SKELETAL: General > Osteopenia | HP:0000938 | T2428 | |
phenodb:1404 | SKELETAL: General > Osteopetrosis | HP:0011002 | T2432 | |
phenodb:1405 | SKELETAL: General > Osteoporosis | HP:0000939 | T2427 | |
phenodb:1406 | SKELETAL: General > Osteosclerosis | HP:0011001 | T2434 | |
phenodb:1407 | SKELETAL: General > Pain | HP:0002653 | T2461 | |
phenodb:1408 | SKELETAL: General > Rickets | HP:0002748 | T2429 | |
phenodb:3228 | SKELETAL: General > Anomaly of cartilage | HP:0002763 | T2487 | |
phenodb:3230 | SKELETAL: General > Anomaly of cartilage > Calcification of cartilage | HP:0100593 | T2519 | |
phenodb:3231 | SKELETAL: General > Anomaly of cartilage > Chondritis | HP:0100662 | T2504 | |
phenodb:3232 | SKELETAL: General > Anomaly of cartilage > Chondrodysplasia punctata | |||
phenodb:3233 | SKELETAL: General > Anomaly of cartilage > Chondrolysis | HP:0100773 | T2494 | |
phenodb:3229 | SKELETAL: General > Anomaly of cartilage > Synovitis | HP:0100769 | T2490 | |
phenodb:3234 | SKELETAL: General > Anomaly of cartilage > Other feature | |||
phenodb:1409 | SKELETAL: Skull | HP:0000929 | ||
phenodb:1410 | SKELETAL: Spine | HP:0000925 | ||
phenodb:1411 | SKELETAL: Spine > General | |||
phenodb:1412 | SKELETAL: Spine > General > Horizontal sacrum | HP:0003440 | ||
phenodb:1413 | SKELETAL: Spine > General > Kyphosis | HP:0002808 | T0806 | |
phenodb:1414 | SKELETAL: Spine > General > Kyphosis > Cervical | HP:0002947 | ||
phenodb:1415 | SKELETAL: Spine > General > Kyphosis > Thoracic | HP:0002942 | ||
phenodb:1416 | SKELETAL: Spine > General > Kyphosis > Other feature | |||
phenodb:1417 | SKELETAL: Spine > General > Lordosis, excessive | HP:0003307 | T0809 | |
phenodb:1418 | SKELETAL: Spine > General > Scoliosis | HP:0002650 | T0810 | |
phenodb:3235 | SKELETAL: Spine > General > Straight | HP:0100795 | T0805 | |
phenodb:3236 | SKELETAL: Spine > General > Rigid | HP:0003306 | T0812 | |
phenodb:2888 | SKELETAL: Spine > General > Other feature | |||
phenodb:1419 | SKELETAL: Spine > Vertebrae | HP:0003468 | ||
phenodb:1422 | SKELETAL: Spine > Vertebrae > Anomalies, NOS | HP:0003312 | T0815 | |
phenodb:1420 | SKELETAL: Spine > Vertebrae > Anterior beaking | HP:0004568 | T0820 | |
phenodb:3237 | SKELETAL: Spine > Vertebrae > Atlanto-axial abnormality | HP:0003413 | T0802 | |
phenodb:1421 | SKELETAL: Spine > Vertebrae > Atlanto-axial instability | HP:0003467 | T0803 | |
phenodb:1423 | SKELETAL: Spine > Vertebrae > Biconcave | HP:0004586 | T0822 | |
phenodb:1424 | SKELETAL: Spine > Vertebrae > Coronal cleft(s) | HP:0003417 | T0816 | |
phenodb:3238 | SKELETAL: Spine > Vertebrae > Delayed ossification of vertebral epiphysis | HP:0012711 | T0828 | |
phenodb:1425 | SKELETAL: Spine > Vertebrae > Endplates, irregular | HP:0003301 | T0817 | |
phenodb:1426 | SKELETAL: Spine > Vertebrae > Flat | HP:0005752 | ||
phenodb:1427 | SKELETAL: Spine > Vertebrae > Fused | HP:0002948 | T0835 | |
phenodb:1428 | SKELETAL: Spine > Vertebrae > Fused > Cervical | HP:0002949 | ||
phenodb:1429 | SKELETAL: Spine > Vertebrae > Fused > Thoracic | HP:0030039 | ||
phenodb:1430 | SKELETAL: Spine > Vertebrae > Fused > Lumbar | HP:0030040 | ||
phenodb:1431 | SKELETAL: Spine > Vertebrae > Hemivertebrae | HP:0002937 | T0834 | |
phenodb:1432 | SKELETAL: Spine > Vertebrae > Interpedicular narrowing | HP:0008450 | T0830 | |
phenodb:3239 | SKELETAL: Spine > Vertebrae > Intervertebaral disk anomaly | HP:0005108 | T0829 | |
phenodb:3243 | SKELETAL: Spine > Vertebrae > Intervertebral disc calcification | HP:0005645 | T0831 | |
phenodb:3244 | SKELETAL: Spine > Vertebrae > Intervetebral disk herniation | HP:0008441 | T0832 | |
phenodb:1433 | SKELETAL: Spine > Vertebrae > Klippel-Feil | HP:0004602 | ||
phenodb:1434 | SKELETAL: Spine > Vertebrae > Odontoid hypoplasia | HP:0003311 | T0824 | |
phenodb:1435 | SKELETAL: Spine > Vertebrae > Ovoid | HP:0003300 | T0818 | |
phenodb:1436 | SKELETAL: Spine > Vertebrae > Platyspondyly | HP:0000926 | T0821 | |
phenodb:3242 | SKELETAL: Spine > Vertebrae > Poorly ossified vertebrae | HP:0100856 | T0826 | |
phenodb:3241 | SKELETAL: Spine > Vertebrae > Punctate calcifications of vertebrae | HP:0008420 | T0825 | |
phenodb:1437 | SKELETAL: Spine > Vertebrae > Schmorl's nodes | HP:0030041 | ||
phenodb:1438 | SKELETAL: Spine > Vertebrae > Segmentation defect | HP:0003422 | T0833 | |
phenodb:1439 | SKELETAL: Spine > Vertebrae > Small / Hypoplasia | HP:0008515 | ||
phenodb:1440 | SKELETAL: Spine > Vertebrae > Spina bifda | HP:0002414 | T2101 | |
phenodb:1441 | SKELETAL: Spine > Vertebrae > Spina bifida occulta | HP:0003298 | T0813 | |
phenodb:1442 | SKELETAL: Spine > Vertebrae > Spinal canal stenosis | HP:0003416 | T0814 | |
phenodb:1443 | SKELETAL: Spine > Vertebrae > Spondylolisthesis | HP:0003302 | T2905 | |
phenodb:1444 | SKELETAL: Spine > Vertebrae > Spondylolysis | HP:0003304 | T0801 | |
phenodb:3240 | SKELETAL: Spine > Vertebrae > Tall | HP:0004570 | T0819 | |
phenodb:1445 | SKELETAL: Spine > Vertebrae > Wedge | HP:0008422 | ||
phenodb:2889 | SKELETAL: Spine > Vertebrae > Other feature | |||
phenodb:3245 | SKELETAL: Spine > Sacrum | HP:0005107 | ||
phenodb:3246 | SKELETAL: Spine > Sacrum > Absent | HP:0010305 | T0867 | |
phenodb:3247 | SKELETAL: Spine > Sacrum > Anomaly of the sacroiliac joint | HP:0100781 | T0868 | |
phenodb:3248 | SKELETAL: Spine > Sacrum > Caudal appendage | HP:0002825 | T0862 | |
phenodb:3249 | SKELETAL: Spine > Sacrum > Pilonidal cyst | HP:0010769 | T0866 | |
phenodb:3607 | SKELETAL: Spine > Sacrum > Other feature | |||
phenodb:1446 | SKELETAL: Chest | HP:0000765 | ||
phenodb:1447 | SKELETAL: Pelvis | HP:0002644 | T0836 | |
phenodb:1448 | SKELETAL: Pelvis > General | HP:0002644 | ||
phenodb:3250 | SKELETAL: Pelvis > General > Asymmetric | HP:0010453 | T0846 | |
phenodb:3251 | SKELETAL: Pelvis > General > Large | HP:0010779 | T0850 | |
phenodb:1449 | SKELETAL: Pelvis > General > Narrow | HP:0003275 | T0840 | |
phenodb:1450 | SKELETAL: Pelvis > General > Small | HP:0008839 | T0839 | |
phenodb:1451 | SKELETAL: Pelvis > General > Other feature | |||
phenodb:1452 | SKELETAL: Pelvis > Acetabulum | HP:0003170 | T0853 | |
phenodb:1453 | SKELETAL: Pelvis > Acetabulum > Flat | HP:0003180 | T0855 | |
phenodb:1454 | SKELETAL: Pelvis > Acetabulum > Horizontal | HP:0003180 | ||
phenodb:1455 | SKELETAL: Pelvis > Acetabulum > Hypoplastic | HP:0003274 | T0857 | |
phenodb:1456 | SKELETAL: Pelvis > Acetabulum > Protrusio | HP:0003179 | T0869 | |
phenodb:3252 | SKELETAL: Pelvis > Acetabulum > Steep | HP:0010455 | T0856 | |
phenodb:1457 | SKELETAL: Pelvis > Acetabulum > Other feature | |||
phenodb:1458 | SKELETAL: Pelvis > Ilium | HP:0002867 | ||
phenodb:1459 | SKELETAL: Pelvis > Ilium > Flared wings | HP:0002869 | T0841 | |
phenodb:1460 | SKELETAL: Pelvis > Ilium > Horns | HP:0009780 | T0851 | |
phenodb:1461 | SKELETAL: Pelvis > Ilium > Hypoplastic | HP:0002866 | T0842 | |
phenodb:1462 | SKELETAL: Pelvis > Ilium > Narrow sacroiliac notch | HP:0008803 | T0860 | |
phenodb:1463 | SKELETAL: Pelvis > Ilium > Narrow wings | HP:0002868 | T0838 | |
phenodb:1464 | SKELETAL: Pelvis > Ilium > Other feature | |||
phenodb:1465 | SKELETAL: Pelvis > Ischium | HP:0003174 | T0848 | |
phenodb:1466 | SKELETAL: Pelvis > Ischium > Hypoplastic | HP:0003175 | T0844 | |
phenodb:1467 | SKELETAL: Pelvis > Ischium > Vertical | |||
phenodb:1468 | SKELETAL: Pelvis > Ischium > Other feature | |||
phenodb:1469 | SKELETAL: Pelvis > Pubis | HP:0003172 | T0837 | |
phenodb:3253 | SKELETAL: Pelvis > Pubis > Abnormal ossification of the pubic bone | HP:0009105 | T0804 | |
phenodb:1470 | SKELETAL: Pelvis > Pubis > Delayed ossification | HP:0008788 | ||
phenodb:1471 | SKELETAL: Pelvis > Pubis > Hypoplastic | HP:0003173 | T0847 | |
phenodb:1472 | SKELETAL: Pelvis > Pubis > Incompleted ossification | HP:0030042 | ||
phenodb:1473 | SKELETAL: Pelvis > Pubis > Wide symphysis | HP:0003183 | T0863 | |
phenodb:1474 | SKELETAL: Pelvis > Pubis > Other feature | |||
phenodb:1475 | SKELETAL: Pelvis > Hips | HP:0003272 | ||
phenodb:1476 | SKELETAL: Pelvis > Hips > Dislocation | HP:0002827 | ||
phenodb:1477 | SKELETAL: Pelvis > Hips > Coxa valga | HP:0002673 | T2513 | |
phenodb:1478 | SKELETAL: Pelvis > Hips > Coxa vara | HP:0002812 | T2515 | |
phenodb:1479 | SKELETAL: Pelvis > Hips > Dysplasia | HP:0001385 | ||
phenodb:1480 | SKELETAL: Pelvis > Hips > Slipped capital femoral epiphyses | HP:0006461 | ||
phenodb:1481 | SKELETAL: Pelvis > Hips > Subluxation | HP:0030043 | ||
phenodb:1482 | SKELETAL: Pelvis > Hips > Other feature | |||
phenodb:1483 | SKELETAL: Limbs, General | HP:0040064 | T0892 | |
phenodb:1484 | SKELETAL: Limbs, General > Acromelia | HP:0010884 | T0893 | |
phenodb:1485 | SKELETAL: Limbs, General > Acromesomelia | HP:0003086 | T0917 | |
phenodb:1486 | SKELETAL: Limbs, General > Amelia | HP:0009827 | T0933 | |
phenodb:1487 | SKELETAL: Limbs, General > Arthralgia | HP:0002829 | T2488 | |
phenodb:2916 | SKELETAL: Limbs, General > Arthritis | HP:0001369 | T2491 | |
phenodb:3254 | SKELETAL: Limbs, General > Arthrogryposis multiplex congenita | HP:0002804 | T0940 | |
phenodb:3672 | SKELETAL: Limbs, General > Distal arthrogryposis | HP:0005684 | T0941 | |
phenodb:1488 | SKELETAL: Limbs, General > Deformity, NOS | |||
phenodb:1489 | SKELETAL: Limbs, General > Long bones | HP:0011314 | ||
phenodb:1493 | SKELETAL: Limbs, General > Long bones > Bowed (aka Curved) | HP:0006487 | T2481 | |
phenodb:1492 | SKELETAL: Limbs, General > Long bones > Long | |||
phenodb:1490 | SKELETAL: Limbs, General > Long bones > Short | HP:0003026 | T0915 | |
phenodb:1491 | SKELETAL: Limbs, General > Long bones > Slender | HP:0003100 | ||
phenodb:1494 | SKELETAL: Limbs, General > Long bones > Other feature | |||
phenodb:3255 | SKELETAL: Limbs, General > Mesomelia | HP:0003027 | T0926 | |
phenodb:1495 | SKELETAL: Limbs, General > Micromelia | HP:0002983 | T0914 | |
phenodb:1496 | SKELETAL: Limbs, General > Phocomelia | HP:0009829 | T0934 | |
phenodb:3256 | SKELETAL: Limbs, General > Pterygia | HP:0001040 | ||
phenodb:1497 | SKELETAL: Limbs, General > Rhizomelia | HP:0008905 | T0921 | |
phenodb:3257 | SKELETAL: Limbs, General > Short limbs | HP:0009826 | T0913 | |
phenodb:3258 | SKELETAL: Limbs, General > Tetraamelia | HP:0003057 | T0932 | |
phenodb:2890 | SKELETAL: Limbs, General > Other feature | |||
phenodb:1498 | SKELETAL: Arms | HP:0002817 | T0949 | |
phenodb:3673 | SKELETAL: Arms > Acromelia | HP:0010482 | T0918 | |
phenodb:3260 | SKELETAL: Arms > Asymmetry | HP:0100560 | T0951 | |
phenodb:1499 | SKELETAL: Arms > Elbow | HP:0009811 | T0983 | |
phenodb:3263 | SKELETAL: Arms > Elbow > Anomaly of the humeroradial joint | HP:0100744 | T0990 | |
phenodb:3267 | SKELETAL: Arms > Elbow > Antecubital pterygium | HP:0009760 | T0947 | |
phenodb:1500 | SKELETAL: Arms > Elbow > Cubitus valgus | HP:0002967 | T0991 | |
phenodb:1501 | SKELETAL: Arms > Elbow > Decreased extension | HP:0001377 | T0985 | |
phenodb:3264 | SKELETAL: Arms > Elbow > Dislocated | HP:0003042 | T2508 | |
phenodb:1502 | SKELETAL: Arms > Elbow > Fixed, fused | HP:0006471 | ||
phenodb:3265 | SKELETAL: Arms > Elbow > Limited flexion | HP:0006376 | T0986 | |
phenodb:3266 | SKELETAL: Arms > Elbow > Limited pronation/supination | HP:0006394 | T0984 | |
phenodb:1503 | SKELETAL: Arms > Elbow > Other feature | |||
phenodb:3268 | SKELETAL: Arms > Forearm | HP:0002973 | T0971 | |
phenodb:1504 | SKELETAL: Arms > Forearm > Forearms, short (mesomelia) | HP:0005011 | T0925 | |
phenodb:3261 | SKELETAL: Arms > Hemiatrophy | HP:0100558 | T0952 | |
phenodb:3259 | SKELETAL: Arms > Hemihypertrophy | |||
phenodb:1505 | SKELETAL: Arms > Humerus | HP:0003063 | T0964 | |
phenodb:3269 | SKELETAL: Arms > Humerus > Absent | HP:0003862 | T0965 | |
phenodb:3270 | SKELETAL: Arms > Humerus > Bifid | HP:0003864 | T0969 | |
phenodb:3271 | SKELETAL: Arms > Humerus > Bowed (aka Curved) | HP:0003865 | T0970 | |
phenodb:1506 | SKELETAL: Arms > Humerus > Fusion / Synostosis with radius | HP:0003041 | T0988 | |
phenodb:1507 | SKELETAL: Arms > Humerus > Hypoplastic | HP:0006507 | ||
phenodb:1508 | SKELETAL: Arms > Humerus > Short | HP:0005792 | T0968 | |
phenodb:1509 | SKELETAL: Arms > Humerus > Other feature | |||
phenodb:1510 | SKELETAL: Arms > Madelung deformity | HP:0003067 | T1003 | |
phenodb:1511 | SKELETAL: Arms > Radius | HP:0002818 | T0972 | |
phenodb:1512 | SKELETAL: Arms > Radius > Aplasia | HP:0003974 | T0973 | |
phenodb:1513 | SKELETAL: Arms > Radius > Bowing | HP:0002986 | T0975 | |
phenodb:1514 | SKELETAL: Arms > Radius > Dislocation, head | HP:0003083 | T2509 | |
phenodb:1515 | SKELETAL: Arms > Radius > Fusion / Synostosis, with ulna | HP:0005037 | T0987 | |
phenodb:1516 | SKELETAL: Arms > Radius > Hypoplasia | HP:0002984 | ||
phenodb:1517 | SKELETAL: Arms > Radius > Short | HP:0002984 | T0974 | |
phenodb:1518 | SKELETAL: Arms > Radius > Other feature | |||
phenodb:3262 | SKELETAL: Arms > Rhizomelic arm shortening | HP:0004991 | T0923 | |
phenodb:1519 | SKELETAL: Arms > Shoulder | HP:0003043 | ||
phenodb:1520 | SKELETAL: Arms > Shoulder > Contracture | HP:0006467 | T0956 | |
phenodb:1521 | SKELETAL: Arms > Shoulder > Dislocation | HP:0003834 | T2510 | |
phenodb:3272 | SKELETAL: Arms > Shoulder > Synostosis | HP:0006595 | T0955 | |
phenodb:1522 | SKELETAL: Arms > Shoulder > Other feature | |||
phenodb:1523 | SKELETAL: Arms > Ulna | HP:0002997 | T0979 | |
phenodb:3273 | SKELETAL: Arms > Ulna > Absent | HP:0003982 | T0978 | |
phenodb:1524 | SKELETAL: Arms > Ulna > Bowing | HP:0003031 | ||
phenodb:1525 | SKELETAL: Arms > Ulna > Hypoplasia | HP:0003022 | ||
phenodb:1526 | SKELETAL: Arms > Ulna > Short | HP:0003022 | T0980 | |
phenodb:1527 | SKELETAL: Arms > Ulna > Other feature | |||
phenodb:1528 | SKELETAL: Arms > Wrist | HP:0003019 | T0992 | |
phenodb:1529 | SKELETAL: Arms > Wrist > Decreased range of motion | HP:0006248 | T0996 | |
phenodb:3274 | SKELETAL: Arms > Wrist > Dislocated | HP:0003994 | T0998 | |
phenodb:1530 | SKELETAL: Arms > Wrist > Flexion contracture | HP:0001239 | T0993 | |
phenodb:1531 | SKELETAL: Arms > Wrist > Other feature | |||
phenodb:1532 | SKELETAL: Hands | HP:0001155 | T1004 | |
phenodb:1533 | SKELETAL: Hands > General | |||
phenodb:3275 | SKELETAL: Hands > General > Absent hand | HP:0004050 | T1010 | |
phenodb:3276 | SKELETAL: Hands > General > Arthrogryposis | HP:0005612 | ||
phenodb:1534 | SKELETAL: Hands > General > Claw hand | HP:0001171 | T1019 | |
phenodb:1535 | SKELETAL: Hands > General > Contractures | HP:0009473 | T1005 | |
phenodb:1536 | SKELETAL: Hands > General > Ectrodactyly | HP:0100257 | cebcbf647380bc37 | |
phenodb:3277 | SKELETAL: Hands > General > Edema | HP:0007514 | T1007 | |
phenodb:1537 | SKELETAL: Hands > General > Large | HP:0001176 | 7515f487e834719e | |
phenodb:1538 | SKELETAL: Hands > General > Small | HP:0001169 | 451aad78795592cd | |
phenodb:3278 | SKELETAL: Hands > General > Radial deviation of the hand | HP:0009486 | T1011 | |
phenodb:3279 | SKELETAL: Hands > General > Trident | HP:0004060 | T1017 | |
phenodb:1539 | SKELETAL: Hands > General > Ulnar deviation | HP:0009487 | T1074 | |
phenodb:1540 | SKELETAL: Hands > General > Other feature | |||
phenodb:1541 | SKELETAL: Hands > Carpals | HP:0011921 | ||
phenodb:1542 | SKELETAL: Hands > Carpals > Advanced ossification, maturation | HP:0004233 | ||
phenodb:1543 | SKELETAL: Hands > Carpals > Delayed ossification, maturation | HP:0001216 | T1001 | |
phenodb:1544 | SKELETAL: Hands > Carpals > Fused | HP:0009702 | T1000 | |
phenodb:3280 | SKELETAL: Hands > Carpals > Osteolysis | HP:0001495 | T0994 | |
phenodb:1545 | SKELETAL: Hands > Carpals > Small | HP:0001498 | T0995 | |
phenodb:1546 | SKELETAL: Hands > Carpals > Other feature | |||
phenodb:1547 | SKELETAL: Hands > Digits / Fingers | HP:0001167 | T0901 | |
phenodb:3297 | SKELETAL: Hands > Digits / Fingers > Absent fingers | HP:0009380 | T0936 | |
phenodb:3296 | SKELETAL: Hands > Digits / Fingers > Absent phalangeal crease | HP:0006109 | T0911 | |
phenodb:1548 | SKELETAL: Hands > Digits / Fingers > Acroosteolysis | HP:0009771 | T2454 | |
phenodb:1549 | SKELETAL: Hands > Digits / Fingers > Arachnodactyly | HP:0001166 | T0930 | 41535e8ed3dc9076 |
phenodb:3281 | SKELETAL: Hands > Digits / Fingers > Bifid phalanx | |||
phenodb:1550 | SKELETAL: Hands > Digits / Fingers > Bifid terminal phalanges | HP:0009883 | T1009 | |
phenodb:1551 | SKELETAL: Hands > Digits / Fingers > Brachydactyly | HP:0001156 | ||
phenodb:1552 | SKELETAL: Hands > Digits / Fingers > Broad | HP:0001500 | c7d8fcc2cb918096 | |
phenodb:3282 | SKELETAL: Hands > Digits / Fingers > Broad fingertips | HP:0011300 | ||
phenodb:3283 | SKELETAL: Hands > Digits / Fingers > Broad phalanx | HP:0006009 | T0900 | |
phenodb:1553 | SKELETAL: Hands > Digits / Fingers > Camptodactyly | HP:0100490 | T1066 | e2dc697e402380a8 |
phenodb:1554 | SKELETAL: Hands > Digits / Fingers > Clinodactyly, 5th finger | HP:0004209 | T1070 | 483af428f909c76c |
phenodb:1555 | SKELETAL: Hands > Digits / Fingers > Clubbing | HP:0100759 | T1047 | 1fbad6d7c48c6989 |
phenodb:1556 | SKELETAL: Hands > Digits / Fingers > Contractures | HP:0030044 | ||
phenodb:3674 | SKELETAL: Hands > Digits / Fingers > Dermatoglyphic abnormality | HP:0007477 | T1039 | |
phenodb:1557 | SKELETAL: Hands > Digits / Fingers > Fetal fingertip pads | HP:0011298 | T0898 | bf858e24ede407d7 |
phenodb:1558 | SKELETAL: Hands > Digits / Fingers > Hyperextensible | HP:0001187 | ||
phenodb:3284 | SKELETAL: Hands > Digits / Fingers > Hypoplastic phalanx | |||
phenodb:3285 | SKELETAL: Hands > Digits / Fingers > Long fingers | HP:0100807 | T0928 | |
phenodb:3286 | SKELETAL: Hands > Digits / Fingers > Macrodactyly | HP:0004099 | T0908 | |
phenodb:1559 | SKELETAL: Hands > Digits / Fingers > Oligodactyly | HP:0001180 | 3bb74018b943c188 | |
phenodb:1560 | SKELETAL: Hands > Digits / Fingers > Overlapping | HP:0010557 | T1072 | 6d82cc5a5f23eb61 |
phenodb:1561 | SKELETAL: Hands > Digits / Fingers > Polydactyly | HP:0001161 | T1054 | |
phenodb:1562 | SKELETAL: Hands > Digits / Fingers > Polydactyly > Mesaxial | HP:0006159 | 2d1d0cff9193cd89 | |
phenodb:1563 | SKELETAL: Hands > Digits / Fingers > Polydactyly > Postaxial | HP:0001162 | T1058 | 6283a01c833da3a0 |
phenodb:1564 | SKELETAL: Hands > Digits / Fingers > Polydactyly > Preaxial | HP:0100258 | 03de7eef71b03368 | |
phenodb:3287 | SKELETAL: Hands > Digits / Fingers > Pseudoepiphyses of the phalanges of the hand | HP:0010235 | T1049 | |
phenodb:3288 | SKELETAL: Hands > Digits / Fingers > Radial deviation of the finger | HP:0009466 | T1008 | |
phenodb:1565 | SKELETAL: Hands > Digits / Fingers > Short fingers | HP:0011927 | T0904 | 1f410b8fecf151fa |
phenodb:3289 | SKELETAL: Hands > Digits / Fingers > Partial absence of finger | HP:0011299 | T0937 | |
phenodb:3290 | SKELETAL: Hands > Digits / Fingers > Short distal phalanx of finger | HP:0009882 | T1046 | |
phenodb:3291 | SKELETAL: Hands > Digits / Fingers > Short phalanges | HP:0009803 | T1012 | |
phenodb:3292 | SKELETAL: Hands > Digits / Fingers > Slender | HP:0001238 | ||
phenodb:3293 | SKELETAL: Hands > Digits / Fingers > Symphalagism | HP:0009700 | T1052 | |
phenodb:1566 | SKELETAL: Hands > Digits / Fingers > Syndactyly | HP:0001159 | c70eafe652dbba67 | |
phenodb:3294 | SKELETAL: Hands > Digits / Fingers > Syndactyly > Cutaneous | HP:0100554 | T0950 | |
phenodb:3295 | SKELETAL: Hands > Digits / Fingers > Syndactyly > Osseous | HP:0010492 | T1051 | |
phenodb:1567 | SKELETAL: Hands > Digits / Fingers > Tapered | HP:0001182 | T1044 | |
phenodb:3298 | SKELETAL: Hands > Digits / Fingers > Ulnar deviation of finger | HP:0009465 | T1073 | |
phenodb:2891 | SKELETAL: Hands > Digits / Fingers > Other feature | |||
phenodb:3299 | SKELETAL: Hands > Metacarpals | HP:0001163 | T1022 | |
phenodb:3305 | SKELETAL: Hands > Metacarpals > Absent | HP:0010048 | T1033 | |
phenodb:3304 | SKELETAL: Hands > Metacarpals > Broad | HP:0001230 | T1031 | |
phenodb:3300 | SKELETAL: Hands > Metacarpals > Long | HP:0010493 | T1028 | |
phenodb:1570 | SKELETAL: Hands > Metacarpals > Short | HP:0010049 | T1023 | |
phenodb:3302 | SKELETAL: Hands > Metacarpals > Short fifth | HP:0010047 | T1025 | |
phenodb:3301 | SKELETAL: Hands > Metacarpals > Short fourth | HP:0010044 | T1021 | |
phenodb:3303 | SKELETAL: Hands > Metacarpals > Synostosis | HP:0009701 | T1029 | |
phenodb:3608 | SKELETAL: Hands > Metacarpals > Other feature | |||
phenodb:1568 | SKELETAL: Hands > Palms | HP:0100871 | ||
phenodb:1569 | SKELETAL: Hands > Palms > Broad | HP:0001169 | T1014 | f69882f3e0ffe9df |
phenodb:1572 | SKELETAL: Hands > Palms > Hypothenar hypoplasia | HP:0010487 | T1040 | a11fc3b105004e89 |
phenodb:3306 | SKELETAL: Hands > Palms > Long | HP:0011302 | T1016 | |
phenodb:2917 | SKELETAL: Hands > Palms > Short | HP:0004279 | T1013 | 861854a2beef4669 |
phenodb:1571 | SKELETAL: Hands > Palms > Single transverse palmar crease(s) | HP:0000954 | T1038 | de4b544c7ed3ad26 |
phenodb:1573 | SKELETAL: Hands > Palms > Thenar hypoplasia | HP:0001245 | T1041 | 94397cb38ffc70aa |
phenodb:3609 | SKELETAL: Hands > Palms > Other feature | |||
phenodb:3307 | SKELETAL: Hands > Palmar Creases | HP:0004334 | T1034 | |
phenodb:3308 | SKELETAL: Hands > Palmar Creases > Absent | HP:0010489 | T1035 | |
phenodb:3309 | SKELETAL: Hands > Palmar Creases > Deep | HP:0006191 | T1036 | |
phenodb:1574 | SKELETAL: Hands > Palmar Creases > Other feature | |||
phenodb:1575 | SKELETAL: Hands > Thumbs | HP:0001172 | ||
phenodb:1576 | SKELETAL: Hands > Thumbs > Absent | HP:0009777 | T1076 | 901e03be3fdf0a9e |
phenodb:1577 | SKELETAL: Hands > Thumbs > Adducted | HP:0001181 | T1083 | 04c423ff6b42ca46 |
phenodb:1578 | SKELETAL: Hands > Thumbs > Bifid distal phalanx | HP:0009944 | T1086 | |
phenodb:3310 | SKELETAL: Hands > Thumbs > Bifid proximal phalanx of the thumb | HP:0009614 | ||
phenodb:1579 | SKELETAL: Hands > Thumbs > Broad | HP:0011304 | T1079 | e97d55e4fb28e608 |
phenodb:1580 | SKELETAL: Hands > Thumbs > Hitchhiker | HP:0001234 | T1078 | 7983ce06c92a2901 |
phenodb:3311 | SKELETAL: Hands > Thumbs > Hypoplastic thumb | HP:0009601 | ||
phenodb:1581 | SKELETAL: Hands > Thumbs > Metacarpal, first short | HP:0010034 | T1030 | |
phenodb:1582 | SKELETAL: Hands > Thumbs > Proximally placed | HP:0009623 | T1081 | 0c0cf943952f9447 |
phenodb:1583 | SKELETAL: Hands > Thumbs > Short | HP:0009778 | T0899 | |
phenodb:1584 | SKELETAL: Hands > Thumbs > Triphalangeal | HP:0001199 | T1080 | eeb336af09f96ae8 |
phenodb:1585 | SKELETAL: Hands > Thumbs > Other feature | |||
phenodb:1586 | SKELETAL: Legs | HP:0002814 | ||
phenodb:3675 | SKELETAL: Legs > Acromelia | HP:0010494 | T0916 | |
phenodb:3314 | SKELETAL: Legs > Asymmetry | HP:0100559 | T1115 | |
phenodb:3312 | SKELETAL: Legs > Edema | HP:0010741 | T1829 | |
phenodb:3317 | SKELETAL: Legs > Femoral hernia | HP:0100541 | T0887 | |
phenodb:3315 | SKELETAL: Legs > Hemiatrophy | HP:0100557 | T1117 | |
phenodb:3316 | SKELETAL: Legs > Hemihypertrophy | HP:0100553 | T1118 | |
phenodb:3313 | SKELETAL: Legs > Sirenomelia | HP:0010497 | T1088 | |
phenodb:3318 | SKELETAL: Legs > Hip | HP:0001384 | ||
phenodb:3319 | SKELETAL: Legs > Hip > Dislocated | HP:0002827 | T2512 | |
phenodb:3320 | SKELETAL: Legs > Hip > Dysplasia | HP:0001385 | T2516 | |
phenodb:3321 | SKELETAL: Legs > Hip > Limited movement | HP:0008800 | T2517 | |
phenodb:3610 | SKELETAL: Legs > Hip > Other feature | |||
phenodb:1587 | SKELETAL: Legs > Femurs | HP:0002823 | T1090 | |
phenodb:3322 | SKELETAL: Legs > Femurs > Absent | HP:0012744 | T1092 | |
phenodb:3323 | SKELETAL: Legs > Femurs > Bifid / Duplicated | HP:0010443 | T1091 | |
phenodb:1588 | SKELETAL: Legs > Femurs > Bowed | HP:0002980 | T1094 | |
phenodb:1589 | SKELETAL: Legs > Femurs > Femoral neck, short | HP:0100864 | T1097 | |
phenodb:1590 | SKELETAL: Legs > Femurs > Hypoplastic | HP:0003097 | T1093 | |
phenodb:3324 | SKELETAL: Legs > Femurs > Slipped femoral capital epiphysis | HP:0006461 | T1096 | |
phenodb:1591 | SKELETAL: Legs > Femurs > Other feature | |||
phenodb:1592 | SKELETAL: Legs > Fibulae | HP:0002991 | T1103 | |
phenodb:1593 | SKELETAL: Legs > Fibulae > Absent | HP:0002990 | T1104 | |
phenodb:3325 | SKELETAL: Legs > Fibulae > Duplicated | HP:0010503 | T0939 | |
phenodb:3326 | SKELETAL: Legs > Fibulae > Hypoplastic | HP:0006492 | ||
phenodb:1594 | SKELETAL: Legs > Fibulae > Serpentine | HP:0030045 | ||
phenodb:1595 | SKELETAL: Legs > Fibulae > Short | HP:0003038 | T1105 | |
phenodb:1596 | SKELETAL: Legs > Fibulae > Long | HP:0003085 | T1106 | |
phenodb:1597 | SKELETAL: Legs > Fibulae > Other feature | |||
phenodb:1598 | SKELETAL: Legs > Knees (genu) | HP:0002815 | T1120 | |
phenodb:1599 | SKELETAL: Legs > Knees (genu) > Contracture | HP:0001371 | T2393 | |
phenodb:3327 | SKELETAL: Legs > Knees (genu) > Dislocated | HP:0004976 | T2507 | |
phenodb:3328 | SKELETAL: Legs > Knees (genu) > Flexion contracture | HP:0006380 | T1123 | |
phenodb:3329 | SKELETAL: Legs > Knees (genu) > Limited movement of the knee | HP:0010501 | T1122 | |
phenodb:1600 | SKELETAL: Legs > Knees (genu) > Pterygium | HP:0001059 | T2502 | |
phenodb:1601 | SKELETAL: Legs > Knees (genu) > Recurvatum | HP:0002816 | T1126 | |
phenodb:1602 | SKELETAL: Legs > Knees (genu) > Valgus | HP:0002857 | T1124 | |
phenodb:1603 | SKELETAL: Legs > Knees (genu) > Varus | HP:0002970 | T1125 | |
phenodb:3330 | SKELETAL: Legs > Knees (genu) > Windswept | HP:0100531 | T1127 | |
phenodb:1604 | SKELETAL: Legs > Knees (genu) > Other feature | |||
phenodb:1605 | SKELETAL: Legs > Patellae | HP:0003045 | T1108 | |
phenodb:1606 | SKELETAL: Legs > Patellae > Absent | HP:0006443 | T1109 | |
phenodb:3331 | SKELETAL: Legs > Patellae > Bipartite | HP:0010498 | T1110 | |
phenodb:1607 | SKELETAL: Legs > Patellae > Dislocated | HP:0002999 | T2511 | |
phenodb:1608 | SKELETAL: Legs > Patellae > Hypoplastic, small | HP:0003065 | T1111 | |
phenodb:1609 | SKELETAL: Legs > Patellae > Other feature | |||
phenodb:1610 | SKELETAL: Legs > Tibia | HP:0002992 | T1098 | |
phenodb:1611 | SKELETAL: Legs > Tibia > Absent | HP:0009556 | T1099 | |
phenodb:1612 | SKELETAL: Legs > Tibia > Bowed | HP:0002982 | T1101 | |
phenodb:3332 | SKELETAL: Legs > Tibia > Hypoplastic | HP:0005736 | T1100 | |
phenodb:3333 | SKELETAL: Legs > Tibia > Long | HP:0010504 | T1102 | |
phenodb:1613 | SKELETAL: Legs > Tibia > Other feature | |||
phenodb:1614 | SKELETAL: Legs > Ankle | HP:0003028 | ||
phenodb:1615 | SKELETAL: Legs > Ankle > Achilles contracture | HP:0001771 | ||
phenodb:3334 | SKELETAL: Legs > Ankle > Contracture | HP:0006466 | T1131 | |
phenodb:3335 | SKELETAL: Legs > Ankle > Limited movement | HP:0010505 | T1129 | |
phenodb:1616 | SKELETAL: Legs > Ankle > Other feature | |||
phenodb:1617 | SKELETAL: Feet | HP:0001760 | T1141 | |
phenodb:1618 | SKELETAL: Feet > General | HP:0001760 | ||
phenodb:3336 | SKELETAL: Feet > General > Absent | HP:0011301 | T1163 | |
phenodb:3337 | SKELETAL: Feet > General > Abnormality of the plantar creases | |||
phenodb:1619 | SKELETAL: Feet > General > Broad | HP:0001769 | T1156 | 86c3214f72d0c4e7 |
phenodb:1620 | SKELETAL: Feet > General > Club | HP:0001883 | T1132 | |
phenodb:1621 | SKELETAL: Feet > General > Deformed, NOS | HP:0001760 | ||
phenodb:1622 | SKELETAL: Feet > General > Ectrodactyly | HP:0100257 | T0903 | 46679495af445c55 |
phenodb:3338 | SKELETAL: Feet > General > Edema | HP:0012098 | T1850 | |
phenodb:1623 | SKELETAL: Feet > General > Equinovarus | HP:0001762 | ||
phenodb:1624 | SKELETAL: Feet > General > Long | HP:0001833 | T1152 | |
phenodb:1625 | SKELETAL: Feet > General > Metatarsus valgus | HP:0010508 | T1133 | 5d170a29ba8032dd |
phenodb:1626 | SKELETAL: Feet > General > Metatarsus varus/adductus | HP:0001840 | T1134 | |
phenodb:3341 | SKELETAL: Feet > General > Narrow | HP:0001786 | T1160 | |
phenodb:3342 | SKELETAL: Feet > General > Pes cavus | HP:0001761 | T1158 | |
phenodb:1627 | SKELETAL: Feet > General > Pes planus | HP:0001763 | T1159 | a071e7b4194e878e |
phenodb:1628 | SKELETAL: Feet > General > Rocker bottom | HP:0001838 | 3b2e4adbadf6bff4 | |
phenodb:1629 | SKELETAL: Feet > General > Small | HP:0001773 | T1161 | |
phenodb:3339 | SKELETAL: Feet > General > Talipes calcaenovalgus | HP:0001884 | ||
phenodb:3340 | SKELETAL: Feet > General > Talipes calcaenovarus | HP:0008124 | T1140 | |
phenodb:3676 | SKELETAL: Feet > General > Talipes equinovalgus | HP:0001772 | T1137 | |
phenodb:1649 | SKELETAL: Feet > General > Talipes equinovarus | HP:0001762 | T1138 | |
phenodb:1630 | SKELETAL: Feet > General > Tarsal bone fusion | HP:0008368 | T1113 | |
phenodb:1631 | SKELETAL: Feet > General > Vertical talus | HP:0001838 | T1157 | |
phenodb:1632 | SKELETAL: Feet > General > Other feature | |||
phenodb:3343 | SKELETAL: Feet > Metatarsals | HP:0001832 | T1149 | |
phenodb:3344 | SKELETAL: Feet > Metatarsals > Short | HP:0010743 | T1177 | |
phenodb:3611 | SKELETAL: Feet > Metatarsals > Other feature | |||
phenodb:3345 | SKELETAL: Feet > Tarsal bones | HP:0001850 | T1112 | |
phenodb:3346 | SKELETAL: Feet > Tarsal bones > Osteolysis | HP:0006234 | T1114 | |
phenodb:3347 | SKELETAL: Feet > Tarsal bones > Talus osteolysis | HP:0008095 | T2906 | |
phenodb:3348 | SKELETAL: Feet > Tarsal bones > Bipartite calcaneus | HP:0008127 | T1150 | |
phenodb:3612 | SKELETAL: Feet > Tarsal bones > Other feature | |||
phenodb:1633 | SKELETAL: Feet > Toes | HP:0001780 | T1144 | |
phenodb:3349 | SKELETAL: Feet > Toes > Absent toes | HP:0010760 | T1168 | |
phenodb:3350 | SKELETAL: Feet > Toes > Partial absence of toe | HP:0011305 | T1181 | |
phenodb:1634 | SKELETAL: Feet > Toes > Acroosteolysis | HP:0001842 | ||
phenodb:1635 | SKELETAL: Feet > Toes > Brachydactyly | HP:0001156 | ||
phenodb:3351 | SKELETAL: Feet > Toes > Broad | HP:0001837 | T1148 | |
phenodb:1636 | SKELETAL: Feet > Toes > Hallux Abnormality | HP:0001844 | T1184 | |
phenodb:3352 | SKELETAL: Feet > Toes > Hallux Abnormality > Absent | HP:0012386 | T1186 | |
phenodb:1637 | SKELETAL: Feet > Toes > Hallux Abnormality > Broad | HP:0010055 | T1189 | 7c222af1a91aae93 |
phenodb:3353 | SKELETAL: Feet > Toes > Hallux Abnormality > Hypoplastic | HP:0008362 | ||
phenodb:3354 | SKELETAL: Feet > Toes > Hallux Abnormality > Long | HP:0001847 | T1187 | |
phenodb:3355 | SKELETAL: Feet > Toes > Hallux Abnormality > Prehensile | |||
phenodb:3356 | SKELETAL: Feet > Toes > Hallux Abnormality > Short | HP:0010109 | T2909 | |
phenodb:1639 | SKELETAL: Feet > Toes > Hallux Abnormality > Valgus | HP:0001822 | T1135 | |
phenodb:3357 | SKELETAL: Feet > Toes > Hallux Abnormality > Varus | HP:0008080 | T1136 | |
phenodb:1640 | SKELETAL: Feet > Toes > Hallux Abnormality > Other feature | |||
phenodb:1638 | SKELETAL: Feet > Toes > Hallux Abnormality > Hammer toe | HP:0001765 | T1170 | 16203d96c596b06c |
phenodb:1641 | SKELETAL: Feet > Toes > Hypoplasia, distal phalangeal segment | HP:0001857 | T1182 | |
phenodb:1642 | SKELETAL: Feet > Toes > Absent / Oligodactyly | HP:0001849 | d0afa3f330b8884b | |
phenodb:1643 | SKELETAL: Feet > Toes > Overlapping | HP:0001845 | T1183 | 14ce1a16018783f4 |
phenodb:3358 | SKELETAL: Feet > Toes > Long | HP:0010511 | T1151 | |
phenodb:3359 | SKELETAL: Feet > Toes > Macrodactyly | HP:0100747 | T1178 | |
phenodb:1644 | SKELETAL: Feet > Toes > Polydactyly | HP:0001829 | T1055 | |
phenodb:1645 | SKELETAL: Feet > Toes > Polydactyly > Mesaxial | HP:0010112 | ||
phenodb:1646 | SKELETAL: Feet > Toes > Polydactyly > Preaxial | HP:0001841 | T1057 | a3552875bb04a6e4 |
phenodb:1647 | SKELETAL: Feet > Toes > Polydactyly > Postaxial | HP:0001830 | T1059 | 108960df1b3f13ae |
phenodb:3613 | SKELETAL: Feet > Toes > Polydactyly > Other feature | |||
phenodb:3360 | SKELETAL: Feet > Toes > Sandal gap | HP:0001852 | T1193 | |
phenodb:3361 | SKELETAL: Feet > Toes > Short | HP:0001831 | T1153 | |
phenodb:1648 | SKELETAL: Feet > Toes > Syndactyly | HP:0001159 | 01f3cc71dd4c3b9d | |
phenodb:3362 | SKELETAL: Feet > Toes > Osseous | HP:0010717 | T1173 | |
phenodb:3363 | SKELETAL: Feet > Toes > Cutaneous | HP:0010621 | T1172 | |
phenodb:3364 | SKELETAL: Feet > Toes > 2-3 toe | HP:0004691 | T1174 | |
phenodb:3365 | SKELETAL: Feet > Toes > 2-4 toe | HP:0010714 | T2908 | |
phenodb:3614 | SKELETAL: Feet > Toes > Other feature | |||
phenodb:2892 | SKELETAL: Feet > Toes > Other feature | |||
phenodb:1650 | MUSCLE, SOFT TISSUE: | |||
phenodb:1651 | MUSCLE, SOFT TISSUE: Muscle | HP:0003011 | ||
phenodb:1652 | MUSCLE, SOFT TISSUE: Muscle > General Abnormalities | |||
phenodb:1653 | MUSCLE, SOFT TISSUE: Muscle > General Abnormalities > Amyotrophy | HP:0003202 | ||
phenodb:1654 | MUSCLE, SOFT TISSUE: Muscle > General Abnormalities > Decreased muscle mass | HP:0003199 | T2401 | |
phenodb:3366 | MUSCLE, SOFT TISSUE: Muscle > General Abnormalities > Muscle agenesis | HP:0100854 | T2395 | |
phenodb:1655 | MUSCLE, SOFT TISSUE: Muscle > General Abnormalities > Muscle atrophy | HP:0003202 | ||
phenodb:3367 | MUSCLE, SOFT TISSUE: Muscle > General Abnormalities > Muscle calcification | HP:0100249 | T2406 | |
phenodb:3368 | MUSCLE, SOFT TISSUE: Muscle > General Abnormalities > Muscle edema | HP:0100748 | T2415 | |
phenodb:3369 | MUSCLE, SOFT TISSUE: Muscle > General Abnormalities > Muscle flaccidity | HP:0010547 | T2376 | |
phenodb:1656 | MUSCLE, SOFT TISSUE: Muscle > General Abnormalities > Muscle hypertrophy, generalized | HP:0003720 | ||
phenodb:1657 | MUSCLE, SOFT TISSUE: Muscle > General Abnormalities > Muscular dystrophy | HP:0003560 | T2396 | |
phenodb:1658 | MUSCLE, SOFT TISSUE: Muscle > General Abnormalities > Myalgia | HP:0003326 | T2405 | |
phenodb:1659 | MUSCLE, SOFT TISSUE: Muscle > General Abnormalities > Myasthenia | HP:0003473 | T2181 | |
phenodb:1660 | MUSCLE, SOFT TISSUE: Muscle > General Abnormalities > Myopathy | HP:0003198 | ||
phenodb:1661 | MUSCLE, SOFT TISSUE: Muscle > General Abnormalities > Myopathy, lipid-storage | |||
phenodb:1662 | MUSCLE, SOFT TISSUE: Muscle > General Abnormalities > Myopathy, myofibrillar | HP:0003715 | T2374 | |
phenodb:3370 | MUSCLE, SOFT TISSUE: Muscle > General Abnormalities > Myositis | HP:0100614 | T2414 | |
phenodb:1663 | MUSCLE, SOFT TISSUE: Muscle > General Abnormalities > Myotonia | HP:0002486 | T2375 | |
phenodb:1664 | MUSCLE, SOFT TISSUE: Muscle > General Abnormalities > Rhabdomyolysis | HP:0003201 | ||
phenodb:1665 | MUSCLE, SOFT TISSUE: Muscle > General Abnormalities > Other feature | |||
phenodb:1666 | MUSCLE, SOFT TISSUE: Muscle > Structure | |||
phenodb:1667 | MUSCLE, SOFT TISSUE: Muscle > Structure > Macroscopic | |||
phenodb:1668 | MUSCLE, SOFT TISSUE: Muscle > Structure > Macroscopic > Calf hypertrophy | HP:0008981 | T2404 | |
phenodb:1669 | MUSCLE, SOFT TISSUE: Muscle > Structure > Macroscopic > Calf muscle pseudohypertrophy | HP:0003707 | ||
phenodb:1671 | MUSCLE, SOFT TISSUE: Muscle > Structure > Macroscopic > Distal muscle atrophy | HP:0003693 | ||
phenodb:1672 | MUSCLE, SOFT TISSUE: Muscle > Structure > Macroscopic > Muscle hypertrophy | HP:0003712 | T2403 | |
phenodb:1673 | MUSCLE, SOFT TISSUE: Muscle > Structure > Macroscopic > Muscle wasting | HP:0003202 | T2397 | |
phenodb:1670 | MUSCLE, SOFT TISSUE: Muscle > Structure > Macroscopic > Proximal muscle atrophy | HP:0007126 | T2400 | |
phenodb:1674 | MUSCLE, SOFT TISSUE: Muscle > Structure > Macroscopic > Other feature | |||
phenodb:1675 | MUSCLE, SOFT TISSUE: Muscle > Structure > Microscopic | |||
phenodb:1676 | MUSCLE, SOFT TISSUE: Muscle > Structure > Microscopic > Centralized nuclei | HP:0003687 | ||
phenodb:1677 | MUSCLE, SOFT TISSUE: Muscle > Structure > Microscopic > Decreased glycosylation of alpha-dystroglycan | HP:0030046 | ||
phenodb:1678 | MUSCLE, SOFT TISSUE: Muscle > Structure > Microscopic > Fiber splitting | HP:0003555 | ||
phenodb:1679 | MUSCLE, SOFT TISSUE: Muscle > Structure > Microscopic > Increased connective tissue | HP:0009025 | ||
phenodb:1680 | MUSCLE, SOFT TISSUE: Muscle > Structure > Microscopic > Increased fatty infiltration | HP:0012548 | ||
phenodb:1681 | MUSCLE, SOFT TISSUE: Muscle > Structure > Microscopic > Increased fiber size variation | HP:0003557 | T2412 | |
phenodb:1682 | MUSCLE, SOFT TISSUE: Muscle > Structure > Microscopic > Internal nuclei | HP:0003687 | ||
phenodb:1683 | MUSCLE, SOFT TISSUE: Muscle > Structure > Microscopic > Multiple mitochondrial DNA (mtDNA) deletions | HP:0003689 | ||
phenodb:1684 | MUSCLE, SOFT TISSUE: Muscle > Structure > Microscopic > Nemaline bodies (rods) on Gomori trichrome staining | HP:0003798 | ||
phenodb:1685 | MUSCLE, SOFT TISSUE: Muscle > Structure > Microscopic > Ragged red fibers | HP:0003200 | ||
phenodb:1686 | MUSCLE, SOFT TISSUE: Muscle > Structure > Microscopic > Rimmed vacuoles | HP:0003805 | ||
phenodb:1687 | MUSCLE, SOFT TISSUE: Muscle > Structure > Microscopic > Subsarcolemmal accumulations of abnormally shaped mitochondria | HP:0003548 | ||
phenodb:1688 | MUSCLE, SOFT TISSUE: Muscle > Structure > Microscopic > Type 1 fiber predominance | HP:0003803 | ||
phenodb:1689 | MUSCLE, SOFT TISSUE: Muscle > Structure > Microscopic > Type 2 fiber atrophy | HP:0003554 | ||
phenodb:1690 | MUSCLE, SOFT TISSUE: Muscle > Structure > Microscopic > Other feature | |||
phenodb:1691 | MUSCLE, SOFT TISSUE: Muscle > Function | |||
phenodb:1695 | MUSCLE, SOFT TISSUE: Muscle > Function > Abnormal EMG | HP:0003457 | T2416 | |
phenodb:1692 | MUSCLE, SOFT TISSUE: Muscle > Function > Difficulty climbing stairs | HP:0003551 | ||
phenodb:1693 | MUSCLE, SOFT TISSUE: Muscle > Function > Difficulty walking | HP:0002355 | ||
phenodb:1694 | MUSCLE, SOFT TISSUE: Muscle > Function > Dysarthria | HP:0001260 | ||
phenodb:1696 | MUSCLE, SOFT TISSUE: Muscle > Function > Exercise intolerance | HP:0003546 | ||
phenodb:1697 | MUSCLE, SOFT TISSUE: Muscle > Function > Fasciculations | HP:0002380 | T2221 | |
phenodb:1698 | MUSCLE, SOFT TISSUE: Muscle > Function > Foot drop | HP:0009027 | ||
phenodb:1699 | MUSCLE, SOFT TISSUE: Muscle > Function > Gower sign | HP:0003391 | T2380 | |
phenodb:1700 | MUSCLE, SOFT TISSUE: Muscle > Function > Hypotonia | HP:0001252 | ||
phenodb:1701 | MUSCLE, SOFT TISSUE: Muscle > Function > Hypotonia, neonatal | HP:0001319 | T2240 | |
phenodb:1702 | MUSCLE, SOFT TISSUE: Muscle > Function > Muscle cramps | HP:0003394 | T2390 | |
phenodb:1703 | MUSCLE, SOFT TISSUE: Muscle > Function > Muscle fatigue | HP:0003750 | T2190 | |
phenodb:3371 | MUSCLE, SOFT TISSUE: Muscle > Function > Muscle hypertonicity (hypertonia) | HP:0001276 | ||
phenodb:1704 | MUSCLE, SOFT TISSUE: Muscle > Function > Muscle rigidity | HP:0002063 | T2243 | |
phenodb:1705 | MUSCLE, SOFT TISSUE: Muscle > Function > Muscle stiffness | HP:0003552 | ||
phenodb:1706 | MUSCLE, SOFT TISSUE: Muscle > Function > Muscle stiffness, with exercise | HP:0008967 | ||
phenodb:1707 | MUSCLE, SOFT TISSUE: Muscle > Function > Muscle weakness | HP:0001324 | ||
phenodb:1708 | MUSCLE, SOFT TISSUE: Muscle > Function > Muscle weakness > Generalized | HP:0003324 | T2379 | |
phenodb:1709 | MUSCLE, SOFT TISSUE: Muscle > Function > Muscle weakness > Distal | HP:0002460 | ||
phenodb:3372 | MUSCLE, SOFT TISSUE: Muscle > Function > Muscle weakness > Distal > Distal lower limb | HP:0009053 | T2383 | |
phenodb:3373 | MUSCLE, SOFT TISSUE: Muscle > Function > Muscle weakness > Distal > Distal upper limb | HP:0008959 | T2384 | |
phenodb:3620 | MUSCLE, SOFT TISSUE: Muscle > Function > Muscle weakness > Distal > Other feature | |||
phenodb:1710 | MUSCLE, SOFT TISSUE: Muscle > Function > Muscle weakness > Facial | HP:0010628 | ||
phenodb:1711 | MUSCLE, SOFT TISSUE: Muscle > Function > Muscle weakness > Hip girdle | HP:0003749 | T2378 | |
phenodb:1712 | MUSCLE, SOFT TISSUE: Muscle > Function > Muscle weakness > Limb-girdle | HP:0003325 | T2386 | |
phenodb:1713 | MUSCLE, SOFT TISSUE: Muscle > Function > Muscle weakness > Proximal | HP:0003701 | ||
phenodb:1714 | MUSCLE, SOFT TISSUE: Muscle > Function > Muscle weakness > Shoulder girdle | HP:0003547 | T2381 | |
phenodb:1715 | MUSCLE, SOFT TISSUE: Muscle > Function > Muscle weakness > Other feature | |||
phenodb:1716 | MUSCLE, SOFT TISSUE: Muscle > Function > Tetany | HP:0001281 | T2392 | |
phenodb:1717 | MUSCLE, SOFT TISSUE: Muscle > Function > Waddling gait | HP:0002515 | T2198 | |
phenodb:2893 | MUSCLE, SOFT TISSUE: Muscle > Function > Other feature | |||
phenodb:1718 | MUSCLE, SOFT TISSUE: Soft tissue | |||
phenodb:3374 | MUSCLE, SOFT TISSUE: Soft tissue > Fasciitis | HP:0100537 | T2413 | |
phenodb:1724 | MUSCLE, SOFT TISSUE: Soft tissue > Increased connective tissue | HP:0009025 | ||
phenodb:3376 | MUSCLE, SOFT TISSUE: Soft tissue > Lipoatrophy | HP:0100578 | T1274 | |
phenodb:1720 | MUSCLE, SOFT TISSUE: Soft tissue > Lipodystrophy | HP:0009125 | T2828 | |
phenodb:1721 | MUSCLE, SOFT TISSUE: Soft tissue > Loss of subcutaneous adipose tissue from extremities / limbs | HP:0003635 | T1201 | |
phenodb:1722 | MUSCLE, SOFT TISSUE: Soft tissue > Loss of subcutaneous adipose tissue from face | HP:0000292 | T2829 | |
phenodb:1723 | MUSCLE, SOFT TISSUE: Soft tissue > Loss of subcutaneous adipose tissue from trunk | HP:0009002 | T2830 | |
phenodb:3375 | MUSCLE, SOFT TISSUE: Soft tissue > Lymphangioma | HP:0100764 | T1848 | |
phenodb:1719 | MUSCLE, SOFT TISSUE: Soft tissue > Lymphedema | HP:0001004 | ||
phenodb:1725 | MUSCLE, SOFT TISSUE: Soft tissue > Minimal subcutaneous fat | HP:0003717 | ||
phenodb:3377 | MUSCLE, SOFT TISSUE: Soft tissue > Subcutaneous calcification | HP:0007618 | T1205 | |
phenodb:3378 | MUSCLE, SOFT TISSUE: Soft tissue > Tendon inflammation | HP:0100686 | T2521 | |
phenodb:3379 | MUSCLE, SOFT TISSUE: Soft tissue > Tendon rupture | HP:0100550 | ||
phenodb:1726 | MUSCLE, SOFT TISSUE: Soft tissue > Other feature | |||
phenodb:1727 | NEUROLOGIC: | HP:0000707 | ||
phenodb:1728 | NEUROLOGIC: Central nervous system | HP:0002011 | ||
phenodb:1729 | NEUROLOGIC: Central nervous system > Structure | |||
phenodb:1730 | NEUROLOGIC: Central nervous system > Structure > Brain, general | |||
phenodb:1731 | NEUROLOGIC: Central nervous system > Structure > Brain, general > Atrophy | HP:0002283 | ||
phenodb:1733 | NEUROLOGIC: Central nervous system > Structure > Brain, general > Large (megalencephaly) | HP:0001355 | T2138 | |
phenodb:1734 | NEUROLOGIC: Central nervous system > Structure > Brain, general > Septo-optic dysplasia | HP:0100842 | T2147 | |
phenodb:3380 | NEUROLOGIC: Central nervous system > Structure > Brain, general > Iron deposition | HP:0012675 | ||
phenodb:1732 | NEUROLOGIC: Central nervous system > Structure > Brain, general > Small | HP:0001322 | ||
phenodb:1735 | NEUROLOGIC: Central nervous system > Structure > Brain, general > Other feature | |||
phenodb:1736 | NEUROLOGIC: Central nervous system > Structure > Cortex | HP:0002538 | ||
phenodb:1737 | NEUROLOGIC: Central nervous system > Structure > Cortex > Agyria | HP:0001339 | ||
phenodb:1738 | NEUROLOGIC: Central nervous system > Structure > Cortex > Arrhinencephaly | HP:0002139 | T2108 | |
phenodb:1740 | NEUROLOGIC: Central nervous system > Structure > Cortex > Arteriovenous malformation | HP:0002408 | ||
phenodb:1739 | NEUROLOGIC: Central nervous system > Structure > Cortex > Astrocytosis | HP:0002446 | ||
phenodb:1741 | NEUROLOGIC: Central nervous system > Structure > Cortex > Autofluorescent lipopigment in neurons | HP:0002074 | ||
phenodb:1746 | NEUROLOGIC: Central nervous system > Structure > Cortex > Cerbral infarction | HP:0002140 | ||
phenodb:1742 | NEUROLOGIC: Central nervous system > Structure > Cortex > Cerebral atrophy | HP:0002059 | T2114 | |
phenodb:1743 | NEUROLOGIC: Central nervous system > Structure > Cortex > Cerebral calcifications | HP:0002514 | T2153 | |
phenodb:1744 | NEUROLOGIC: Central nervous system > Structure > Cortex > Cerebral cysts | HP:0010576 | ||
phenodb:1745 | NEUROLOGIC: Central nervous system > Structure > Cortex > Cerebral edema | HP:0002181 | ||
phenodb:1747 | NEUROLOGIC: Central nervous system > Structure > Cortex > Colpocephaly | HP:0030048 | ||
phenodb:1748 | NEUROLOGIC: Central nervous system > Structure > Cortex > Corpus callosum, absent / agenesis | HP:0001274 | T2131 | |
phenodb:1749 | NEUROLOGIC: Central nervous system > Structure > Cortex > Cortical dysplasia | HP:0002539 | ||
phenodb:1750 | NEUROLOGIC: Central nervous system > Structure > Cortex > Cortical tubers | HP:0009717 | ||
phenodb:1751 | NEUROLOGIC: Central nervous system > Structure > Cortex > Delayed myelination | HP:0002188 | ||
phenodb:1752 | NEUROLOGIC: Central nervous system > Structure > Cortex > Demyelination | HP:0011096 | ||
phenodb:1753 | NEUROLOGIC: Central nervous system > Structure > Cortex > Encephalocele | HP:0002084 | T2097 | |
phenodb:3382 | NEUROLOGIC: Central nervous system > Structure > Cortex > Encephalocele > Anterior encephalocele | HP:0007035 | T2099 | |
phenodb:3621 | NEUROLOGIC: Central nervous system > Structure > Cortex > Encephalocele > Other feature | |||
phenodb:1754 | NEUROLOGIC: Central nervous system > Structure > Cortex > Gliosis | HP:0002171 | ||
phenodb:1755 | NEUROLOGIC: Central nervous system > Structure > Cortex > Heterotopia / Neuronal migration defect | HP:0002282 | T2125 | |
phenodb:1759 | NEUROLOGIC: Central nervous system > Structure > Cortex > Hemorrhage | |||
phenodb:1760 | NEUROLOGIC: Central nervous system > Structure > Cortex > Hemorrhage > Cerebral | HP:0001342 | ||
phenodb:1761 | NEUROLOGIC: Central nervous system > Structure > Cortex > Hemorrhage > Intracranial | HP:0002170 | T2151 | |
phenodb:1762 | NEUROLOGIC: Central nervous system > Structure > Cortex > Hemorrhage > Parenchymal | HP:0001342 | ||
phenodb:1763 | NEUROLOGIC: Central nervous system > Structure > Cortex > Hemorrhage > Subarachnoid | HP:0002138 | ||
phenodb:1764 | NEUROLOGIC: Central nervous system > Structure > Cortex > Hemorrhage > Subdural | HP:0100309 | T2607 | |
phenodb:1765 | NEUROLOGIC: Central nervous system > Structure > Cortex > Hemorrhage > Other feature | |||
phenodb:1756 | NEUROLOGIC: Central nervous system > Structure > Cortex > Holoprosencephaly | HP:0001360 | ||
phenodb:1757 | NEUROLOGIC: Central nervous system > Structure > Cortex > Hydranencephaly | HP:0002324 | T2110 | |
phenodb:1758 | NEUROLOGIC: Central nervous system > Structure > Cortex > Hypomyelination | HP:0003429 | ||
phenodb:1766 | NEUROLOGIC: Central nervous system > Structure > Cortex > Intracranial pressure, increased | HP:0002516 | T2171 | |
phenodb:1767 | NEUROLOGIC: Central nervous system > Structure > Cortex > Ischemic stroke | HP:0002140 | T2168 | |
phenodb:1769 | NEUROLOGIC: Central nervous system > Structure > Cortex > Leukodystrophy | HP:0002415 | ||
phenodb:1770 | NEUROLOGIC: Central nervous system > Structure > Cortex > Leukoencephalopathy | HP:0002352 | ||
phenodb:1768 | NEUROLOGIC: Central nervous system > Structure > Cortex > Lewy bodies | HP:0100315 | ||
phenodb:1771 | NEUROLOGIC: Central nervous system > Structure > Cortex > Lissencephaly | HP:0001339 | T2122 | |
phenodb:1772 | NEUROLOGIC: Central nervous system > Structure > Cortex > Lissencephaly > Smooth | HP:0006818 | ||
phenodb:1773 | NEUROLOGIC: Central nervous system > Structure > Cortex > Lissencephaly > Cobblestone | HP:0007260 | T2129 | |
phenodb:1774 | NEUROLOGIC: Central nervous system > Structure > Cortex > Lissencephaly > Other feature | |||
phenodb:1775 | NEUROLOGIC: Central nervous system > Structure > Cortex > Neurodegeneration | HP:0002180 | ||
phenodb:1776 | NEUROLOGIC: Central nervous system > Structure > Cortex > Neurofibrillary tangles | HP:0002185 | ||
phenodb:1777 | NEUROLOGIC: Central nervous system > Structure > Cortex > Neuronal loss | HP:0002529 | ||
phenodb:1778 | NEUROLOGIC: Central nervous system > Structure > Cortex > Pachygyria | HP:0001302 | T2123 | |
phenodb:1779 | NEUROLOGIC: Central nervous system > Structure > Cortex > Periventricular white matter changes | HP:0006970 | T2420 | |
phenodb:1780 | NEUROLOGIC: Central nervous system > Structure > Cortex > Polymicrogyria | HP:0002126 | T2121 | |
phenodb:1781 | NEUROLOGIC: Central nervous system > Structure > Cortex > Septum pellucidum abnormality | HP:0007375 | ||
phenodb:1782 | NEUROLOGIC: Central nervous system > Structure > Cortex > Septum pellucidum abnormality > Cavum | HP:0002389 | T2419 | |
phenodb:1783 | NEUROLOGIC: Central nervous system > Structure > Cortex > Septum pellucidum abnormality > Absent | HP:0001331 | T2130 | |
phenodb:1784 | NEUROLOGIC: Central nervous system > Structure > Cortex > Septum pellucidum abnormality > Other feature | |||
phenodb:1785 | NEUROLOGIC: Central nervous system > Structure > Cortex > Occipital encephalocele | HP:0002085 | T2098 | |
phenodb:1786 | NEUROLOGIC: Central nervous system > Structure > Cortex > Porencephaly | HP:0002132 | T2137 | |
phenodb:1787 | NEUROLOGIC: Central nervous system > Structure > Cortex > Schizencephaly | HP:0010636 | T2139 | |
phenodb:1788 | NEUROLOGIC: Central nervous system > Structure > Cortex > White matter abnormalities | HP:0002500 | T2421 | |
phenodb:2894 | NEUROLOGIC: Central nervous system > Structure > Cortex > Other feature | |||
phenodb:3381 | NEUROLOGIC: Central nervous system > Structure > Anencephaly | HP:0002323 | T2096 | |
phenodb:1789 | NEUROLOGIC: Central nervous system > Structure > Basal ganglia | |||
phenodb:1790 | NEUROLOGIC: Central nervous system > Structure > Basal ganglia > Abnormalities | HP:0002134 | T2156 | |
phenodb:1791 | NEUROLOGIC: Central nervous system > Structure > Basal ganglia > Calcifications | HP:0002135 | T2155 | |
phenodb:1792 | NEUROLOGIC: Central nervous system > Structure > Basal ganglia > Other feature | |||
phenodb:1793 | NEUROLOGIC: Central nervous system > Structure > Ventricles | HP:0002118 | ||
phenodb:1794 | NEUROLOGIC: Central nervous system > Structure > Ventricles > Aqueductal stenosis | HP:0002410 | T2118 | |
phenodb:1795 | NEUROLOGIC: Central nervous system > Structure > Ventricles > Arnold-Chiari malformation | HP:0002308 | T2120 | |
phenodb:1799 | NEUROLOGIC: Central nervous system > Structure > Ventricles > Choroid plexus calcifications | HP:0006960 | ||
phenodb:1800 | NEUROLOGIC: Central nervous system > Structure > Ventricles > Choroid plexus cysts | HP:0002190 | ||
phenodb:3383 | NEUROLOGIC: Central nervous system > Structure > Ventricles > Communicating hydrocephalus | HP:0001334 | T2117 | |
phenodb:1796 | NEUROLOGIC: Central nervous system > Structure > Ventricles > Dandy-Walker malformation | HP:0001305 | T2119 | |
phenodb:1801 | NEUROLOGIC: Central nervous system > Structure > Ventricles > Hydrocephalus | HP:0000238 | T2115 | |
phenodb:1797 | NEUROLOGIC: Central nervous system > Structure > Ventricles > Subependymal cysts | HP:0002416 | ||
phenodb:1798 | NEUROLOGIC: Central nervous system > Structure > Ventricles > Ventricle, large / Ventriculomegaly | HP:0002119 | ||
phenodb:1802 | NEUROLOGIC: Central nervous system > Structure > Ventricles > Other feature | |||
phenodb:1803 | NEUROLOGIC: Central nervous system > Structure > Cerebellum | HP:0001317 | T2146 | |
phenodb:1804 | NEUROLOGIC: Central nervous system > Structure > Cerebellum > Atrophy | HP:0001272 | T2144 | |
phenodb:1805 | NEUROLOGIC: Central nervous system > Structure > Cerebellum > Cysts | HP:0002350 | ||
phenodb:1806 | NEUROLOGIC: Central nervous system > Structure > Cerebellum > Dysplasia | HP:0007033 | ||
phenodb:1809 | NEUROLOGIC: Central nervous system > Structure > Cerebellum > Cisterna magna, large | HP:0002280 | T2112 | |
phenodb:1810 | NEUROLOGIC: Central nervous system > Structure > Cerebellum > Deep posterior interpeduncular fossa | HP:0100951 | ||
phenodb:1807 | NEUROLOGIC: Central nervous system > Structure > Cerebellum > Hypoplasia | HP:0001321 | T2143 | |
phenodb:1811 | NEUROLOGIC: Central nervous system > Structure > Cerebellum > Molar tooth sign | HP:0002419 | ||
phenodb:1812 | NEUROLOGIC: Central nervous system > Structure > Cerebellum > Other feature | |||
phenodb:3384 | NEUROLOGIC: Central nervous system > Structure > Cerebellar vermis anomaly | HP:0002334 | T2141 | |
phenodb:3385 | NEUROLOGIC: Central nervous system > Structure > Cerebellar vermis anomaly > Cerebellar vermis agenesis | HP:0002335 | ||
phenodb:1808 | NEUROLOGIC: Central nervous system > Structure > Cerebellar vermis anomaly > Cerebellar vermis hypoplasia | HP:0001320 | T2145 | |
phenodb:3622 | NEUROLOGIC: Central nervous system > Structure > Cerebellar vermis anomaly > Other feature | |||
phenodb:1813 | NEUROLOGIC: Central nervous system > Structure > Brain Stem | HP:0002363 | T2134 | |
phenodb:3387 | NEUROLOGIC: Central nervous system > Structure > Brain Stem > Anomaly of the medulla oblongata | HP:0011441 | ||
phenodb:3386 | NEUROLOGIC: Central nervous system > Structure > Brain Stem > Anomaly of the midbrain | HP:0002418 | T2132 | |
phenodb:3388 | NEUROLOGIC: Central nervous system > Structure > Brain Stem > Anomaly of the pons | HP:0007361 | T2135 | |
phenodb:1814 | NEUROLOGIC: Central nervous system > Structure > Brain Stem > Hypoplasia | HP:0007362 | ||
phenodb:1815 | NEUROLOGIC: Central nervous system > Structure > Brain Stem > Hypothalamic hamartoma | HP:0002444 | T2041 | |
phenodb:1816 | NEUROLOGIC: Central nervous system > Structure > Brain Stem > Olivopontocerebellar atrophy / degneration | HP:0002542 | ||
phenodb:1817 | NEUROLOGIC: Central nervous system > Structure > Brain Stem > Pontine hypoplasia | HP:0012110 | ||
phenodb:1818 | NEUROLOGIC: Central nervous system > Structure > Brain Stem > Other feature | |||
phenodb:1819 | NEUROLOGIC: Central nervous system > Structure > Meninges | HP:0010651 | ||
phenodb:1820 | NEUROLOGIC: Central nervous system > Structure > Meninges > Arachnoid abnormalities | HP:0100700 | ||
phenodb:1821 | NEUROLOGIC: Central nervous system > Structure > Meninges > Arachnoid abnormalities > Specify | |||
phenodb:1822 | NEUROLOGIC: Central nervous system > Structure > Meninges > Dura mater abnormalities | HP:0010652 | ||
phenodb:1823 | NEUROLOGIC: Central nervous system > Structure > Meninges > Dura mater abnormalities > Falx calcifications | HP:0005462 | ||
phenodb:1824 | NEUROLOGIC: Central nervous system > Structure > Meninges > Dura mater abnormalities > Other | |||
phenodb:1825 | NEUROLOGIC: Central nervous system > Structure > Meninges > Pia mater Abnormalities | HP:0100701 | ||
phenodb:1826 | NEUROLOGIC: Central nervous system > Structure > Meninges > Pia mater Abnormalities > Specify | |||
phenodb:1827 | NEUROLOGIC: Central nervous system > Structure > Spinal cord | HP:0002143 | ||
phenodb:3389 | NEUROLOGIC: Central nervous system > Structure > Spinal cord > Anomaly of the anterior horn cells | HP:0006802 | T2191 | |
phenodb:1828 | NEUROLOGIC: Central nervous system > Structure > Spinal cord > Cervical cord compression | HP:0002341 | ||
phenodb:1829 | NEUROLOGIC: Central nervous system > Structure > Spinal cord > Cervical myelopathy | HP:0002318 | ||
phenodb:1830 | NEUROLOGIC: Central nervous system > Structure > Spinal cord > Degeneration of the lateral corticospinal tracts | HP:0002314 | ||
phenodb:3390 | NEUROLOGIC: Central nervous system > Structure > Spinal cord > Diastematomyelia | |||
phenodb:1831 | NEUROLOGIC: Central nervous system > Structure > Spinal cord > Dural ectasia | HP:0100775 | T2107 | |
phenodb:1832 | NEUROLOGIC: Central nervous system > Structure > Spinal cord > Meningocele | HP:0002435 | T2100 | |
phenodb:1833 | NEUROLOGIC: Central nervous system > Structure > Spinal cord > Myelomeningocele | HP:0002475 | ||
phenodb:3391 | NEUROLOGIC: Central nervous system > Structure > Spinal cord > Neural tube defect | HP:0010301 | T2095 | |
phenodb:1834 | NEUROLOGIC: Central nervous system > Structure > Spinal cord > Spinal cord compression | HP:0002176 | ||
phenodb:1835 | NEUROLOGIC: Central nervous system > Structure > Spinal cord > Syrinx (AKA syringomyelia) | HP:0003396 | T2106 | |
phenodb:3218 | NEUROLOGIC: Central nervous system > Structure > Spinal cord > Tarlov cyst | |||
phenodb:3392 | NEUROLOGIC: Central nervous system > Structure > Spinal cord > Tethered cord | HP:0002144 | ||
phenodb:1836 | NEUROLOGIC: Central nervous system > Structure > Spinal cord > Vibratory sensation, decreased | HP:0002495 | ||
phenodb:1837 | NEUROLOGIC: Central nervous system > Structure > Spinal cord > Other feature | |||
phenodb:1838 | NEUROLOGIC: Central nervous system > Function | |||
phenodb:1839 | NEUROLOGIC: Central nervous system > Function > General | |||
phenodb:3395 | NEUROLOGIC: Central nervous system > Function > General > Altered level of consciousness | |||
phenodb:1840 | NEUROLOGIC: Central nervous system > Function > General > Autonomic dysfunction | HP:0002459 | T2157 | |
phenodb:3393 | NEUROLOGIC: Central nervous system > Function > General > Autonomic dysfunction > Abnormality of temperature regulation | HP:0004370 | T1211 | |
phenodb:3394 | NEUROLOGIC: Central nervous system > Function > General > Autonomic dysfunction > Heat intolerance | HP:0002046 | T1210 | |
phenodb:1841 | NEUROLOGIC: Central nervous system > Function > General > Autonomic dysfunction > Orthostatic hypotension | HP:0001278 | T1821 | |
phenodb:1842 | NEUROLOGIC: Central nervous system > Function > General > Autonomic dysfunction > Other feature | |||
phenodb:1843 | NEUROLOGIC: Central nervous system > Function > General > Coma | HP:0001259 | T2287 | |
phenodb:1844 | NEUROLOGIC: Central nervous system > Function > General > Confusion | HP:0001289 | ||
phenodb:3396 | NEUROLOGIC: Central nervous system > Function > General > Disorientation | HP:0001289 | T2291 | |
phenodb:1845 | NEUROLOGIC: Central nervous system > Function > General > Encephalopathy | HP:0001298 | ||
phenodb:1846 | NEUROLOGIC: Central nervous system > Function > General > Headache | HP:0002315 | T2166 | |
phenodb:3398 | NEUROLOGIC: Central nervous system > Function > General > Hemiballismus | HP:0009937 | T2226 | |
phenodb:1847 | NEUROLOGIC: Central nervous system > Function > General > Infection | HP:0011450 | ||
phenodb:1848 | NEUROLOGIC: Central nervous system > Function > General > Infection > Abscess | HP:0030049 | ||
phenodb:1849 | NEUROLOGIC: Central nervous system > Function > General > Infection > Encephalitis | HP:0002383 | T2179 | |
phenodb:1850 | NEUROLOGIC: Central nervous system > Function > General > Infection > Meningitis | HP:0001287 | T2180 | |
phenodb:1851 | NEUROLOGIC: Central nervous system > Function > General > Infection > Other feature | |||
phenodb:1852 | NEUROLOGIC: Central nervous system > Function > General > Irritability | HP:0000737 | ||
phenodb:1853 | NEUROLOGIC: Central nervous system > Function > General > Lethargy | HP:0001254 | T2290 | |
phenodb:1854 | NEUROLOGIC: Central nervous system > Function > General > Migraine | HP:0002076 | T2167 | |
phenodb:1855 | NEUROLOGIC: Central nervous system > Function > General > Sleep disturbances | HP:0002360 | T2282 | |
phenodb:3399 | NEUROLOGIC: Central nervous system > Function > General > Sleep disturbances > Hypersomnia | HP:0100786 | T2283 | |
phenodb:1856 | NEUROLOGIC: Central nervous system > Function > General > Sleep disturbances > Insomnia | HP:0100785 | T2285 | |
phenodb:1857 | NEUROLOGIC: Central nervous system > Function > General > Sleep disturbances > Narcolepsy | HP:0030050 | ||
phenodb:1858 | NEUROLOGIC: Central nervous system > Function > General > Sleep disturbances > Restless legs | HP:0012452 | ||
phenodb:1859 | NEUROLOGIC: Central nervous system > Function > General > Sleep disturbances > Other feature | |||
phenodb:3397 | NEUROLOGIC: Central nervous system > Function > General > Somnolence | HP:0001262 | T2284 | |
phenodb:2895 | NEUROLOGIC: Central nervous system > Function > General > Other feature | |||
phenodb:1860 | NEUROLOGIC: Central nervous system > Function > Cranial Nerves | HP:0001291 | ||
phenodb:1861 | NEUROLOGIC: Central nervous system > Function > Cranial Nerves > Anosmia | HP:0000458 | ||
phenodb:1862 | NEUROLOGIC: Central nervous system > Function > Cranial Nerves > Apraxia | HP:0002186 | T2231 | |
phenodb:1863 | NEUROLOGIC: Central nervous system > Function > Cranial Nerves > Bulbar palsy | HP:0001283 | ||
phenodb:1864 | NEUROLOGIC: Central nervous system > Function > Cranial Nerves > Drooling | HP:0002307 | T2182 | |
phenodb:1865 | NEUROLOGIC: Central nervous system > Function > Cranial Nerves > Dysarthria | HP:0001260 | T2302 | |
phenodb:1866 | NEUROLOGIC: Central nervous system > Function > Cranial Nerves > Dysphagia | HP:0002015 | T1416 | |
phenodb:1867 | NEUROLOGIC: Central nervous system > Function > Cranial Nerves > Dysphasia | HP:0002357 | T2295 | |
phenodb:1868 | NEUROLOGIC: Central nervous system > Function > Cranial Nerves > Dysphonia | HP:0001618 | T2303 | |
phenodb:1869 | NEUROLOGIC: Central nervous system > Function > Cranial Nerves > Facial palsy | HP:0010628 | T0108 | |
phenodb:1870 | NEUROLOGIC: Central nervous system > Function > Cranial Nerves > Facial palsy > Unilateral | HP:0012799 | ||
phenodb:1871 | NEUROLOGIC: Central nervous system > Function > Cranial Nerves > Facial palsy > Bilateral | HP:0001349 | ||
phenodb:1872 | NEUROLOGIC: Central nervous system > Function > Cranial Nerves > Nystagmus | HP:0000639 | T0334 | |
phenodb:1873 | NEUROLOGIC: Central nervous system > Function > Cranial Nerves > Palsies | HP:0006824 | ||
phenodb:1874 | NEUROLOGIC: Central nervous system > Function > Cranial Nerves > Palsies > Generalized (feature) | HP:0006824 | ||
phenodb:1875 | NEUROLOGIC: Central nervous system > Function > Cranial Nerves > Palsies > Specify | |||
phenodb:1876 | NEUROLOGIC: Central nervous system > Function > Cranial Nerves > Phonophobia | HP:0002183 | T0622 | |
phenodb:1877 | NEUROLOGIC: Central nervous system > Function > Cranial Nerves > Photophobia | HP:0000613 | T0321 | |
phenodb:3400 | NEUROLOGIC: Central nervous system > Function > Cranial Nerves > Retrobulbar optic neuritis | HP:0100654 | T2160 | |
phenodb:1878 | NEUROLOGIC: Central nervous system > Function > Cranial Nerves > Tongue fasciculations | HP:0001308 | ||
phenodb:1879 | NEUROLOGIC: Central nervous system > Function > Cranial Nerves > Trigeminal neuralgia | HP:0100661 | T2159 | |
phenodb:2896 | NEUROLOGIC: Central nervous system > Function > Cranial Nerves > Other feature | |||
phenodb:1880 | NEUROLOGIC: Central nervous system > Function > Cognition | |||
phenodb:1881 | NEUROLOGIC: Central nervous system > Function > Movement | HP:0100022 | T2202 | |
phenodb:1882 | NEUROLOGIC: Central nervous system > Function > Movement > Akinesia | HP:0002304 | T2230 | |
phenodb:1883 | NEUROLOGIC: Central nervous system > Function > Movement > Ataxia | HP:0001251 | ||
phenodb:3401 | NEUROLOGIC: Central nervous system > Function > Movement > Ataxia > Cerebellar ataxia | HP:0001251 | T2199 | |
phenodb:3402 | NEUROLOGIC: Central nervous system > Function > Movement > Ataxia > Sensory ataxia | HP:0010871 | T2201 | |
phenodb:3623 | NEUROLOGIC: Central nervous system > Function > Movement > Ataxia > Other feature | |||
phenodb:1884 | NEUROLOGIC: Central nervous system > Function > Movement > Athetosis | HP:0002305 | T2211 | |
phenodb:1885 | NEUROLOGIC: Central nervous system > Function > Movement > Axial hypotonia | HP:0011398 | T2236 | |
phenodb:1886 | NEUROLOGIC: Central nervous system > Function > Movement > Bradykinesia | HP:0002067 | T2229 | |
phenodb:1894 | NEUROLOGIC: Central nervous system > Function > Movement > Cerebellar signs | HP:0001317 | ||
phenodb:1895 | NEUROLOGIC: Central nervous system > Function > Movement > Chorea | HP:0002072 | T2209 | |
phenodb:1896 | NEUROLOGIC: Central nervous system > Function > Movement > Choreoathetosis | HP:0001266 | T2210 | |
phenodb:1897 | NEUROLOGIC: Central nervous system > Function > Movement > Cogwheel rigidity | HP:0002396 | ||
phenodb:1898 | NEUROLOGIC: Central nervous system > Function > Movement > Dysdiadochokinesis | HP:0002075 | T2189 | |
phenodb:1899 | NEUROLOGIC: Central nervous system > Function > Movement > Dyskinesia | HP:0100660 | T2203 | |
phenodb:1900 | NEUROLOGIC: Central nervous system > Function > Movement > Dysmetria | HP:0001310 | T2232 | |
phenodb:1901 | NEUROLOGIC: Central nervous system > Function > Movement > Dystonia | HP:0001332 | T2212 | |
phenodb:3403 | NEUROLOGIC: Central nervous system > Function > Movement > Dystonia > Facial dystonia | HP:0012179 | ||
phenodb:1902 | NEUROLOGIC: Central nervous system > Function > Movement > Dystonia > Paroxysmal | HP:0002268 | T2217 | |
phenodb:3404 | NEUROLOGIC: Central nervous system > Function > Movement > Dystonia > Spasmodic torticollis | HP:0000473 | T2493 | |
phenodb:1903 | NEUROLOGIC: Central nervous system > Function > Movement > Dystonia > Torsion | HP:0001304 | T2218 | |
phenodb:1904 | NEUROLOGIC: Central nervous system > Function > Movement > Dystonia > Writer's cramp | HP:0002356 | ||
phenodb:1905 | NEUROLOGIC: Central nervous system > Function > Movement > Dystonia > Other feature | |||
phenodb:1907 | NEUROLOGIC: Central nervous system > Function > Movement > Extrapyramidal signs | HP:0002071 | T2227 | |
phenodb:1887 | NEUROLOGIC: Central nervous system > Function > Movement > Gait | |||
phenodb:1888 | NEUROLOGIC: Central nervous system > Function > Movement > Gait > Abnormalities | HP:0001288 | T2192 | |
phenodb:1889 | NEUROLOGIC: Central nervous system > Function > Movement > Gait > Ataxic | HP:0002066 | ||
phenodb:1890 | NEUROLOGIC: Central nervous system > Function > Movement > Gait > Broad-based | HP:0002136 | T2195 | |
phenodb:1891 | NEUROLOGIC: Central nervous system > Function > Movement > Gait > Shuffling | HP:0002362 | T2194 | |
phenodb:1892 | NEUROLOGIC: Central nervous system > Function > Movement > Gait > Tip-toe | HP:0030051 | ||
phenodb:1893 | NEUROLOGIC: Central nervous system > Function > Movement > Gait > Other feature | |||
phenodb:1908 | NEUROLOGIC: Central nervous system > Function > Movement > Hemiparesis | HP:0001269 | T2256 | |
phenodb:1909 | NEUROLOGIC: Central nervous system > Function > Movement > Hemiplegia | HP:0002301 | T2257 | |
phenodb:3405 | NEUROLOGIC: Central nervous system > Function > Movement > Hyperkinesia | HP:0002487 | T2334 | |
phenodb:1910 | NEUROLOGIC: Central nervous system > Function > Movement > Hypertonia | HP:0001276 | T2242 | |
phenodb:1906 | NEUROLOGIC: Central nervous system > Function > Movement > Hypokinesia | HP:0002375 | T2187 | |
phenodb:1911 | NEUROLOGIC: Central nervous system > Function > Movement > Hypotonia | HP:0001252 | T2234 | |
phenodb:1912 | NEUROLOGIC: Central nervous system > Function > Movement > Inability to walk | HP:0002540 | ||
phenodb:3406 | NEUROLOGIC: Central nervous system > Function > Movement > Incoordination | HP:0002311 | ||
phenodb:1913 | NEUROLOGIC: Central nervous system > Function > Movement > Lower limb spasticity | HP:0002061 | T2251 | |
phenodb:1914 | NEUROLOGIC: Central nervous system > Function > Movement > Lower limb weakness | HP:0007340 | ||
phenodb:3407 | NEUROLOGIC: Central nervous system > Function > Movement > Motor tic | HP:0100034 | T2222 | |
phenodb:1915 | NEUROLOGIC: Central nervous system > Function > Movement > Myoclonus | HP:0001336 | ||
phenodb:1916 | NEUROLOGIC: Central nervous system > Function > Movement > Opisthotonus | HP:0002179 | T2388 | |
phenodb:1917 | NEUROLOGIC: Central nervous system > Function > Movement > Orofacial dyskinesia | HP:0002310 | ||
phenodb:1918 | NEUROLOGIC: Central nervous system > Function > Movement > Paraparesis | HP:0002385 | T2183 | |
phenodb:1919 | NEUROLOGIC: Central nervous system > Function > Movement > Parkinsonism | HP:0001300 | ||
phenodb:1920 | NEUROLOGIC: Central nervous system > Function > Movement > Postural instability | HP:0002172 | T2193 | |
phenodb:1921 | NEUROLOGIC: Central nervous system > Function > Movement > Pyramidal signs | HP:0007256 | T2228 | |
phenodb:1922 | NEUROLOGIC: Central nervous system > Function > Movement > Rigidity | HP:0002063 | ||
phenodb:1923 | NEUROLOGIC: Central nervous system > Function > Movement > Scanning speech | HP:0002168 | T2300 | |
phenodb:1924 | NEUROLOGIC: Central nervous system > Function > Movement > Spastic diplegia | HP:0001264 | T2185 | |
phenodb:1925 | NEUROLOGIC: Central nervous system > Function > Movement > Spastic gait | HP:0002064 | T2196 | |
phenodb:1926 | NEUROLOGIC: Central nervous system > Function > Movement > Spastic paraparesis | HP:0002313 | ||
phenodb:1927 | NEUROLOGIC: Central nervous system > Function > Movement > Spastic paraplegia | HP:0001258 | T2184 | |
phenodb:1928 | NEUROLOGIC: Central nervous system > Function > Movement > Spastic quadriparesis | HP:0001285 | ||
phenodb:1929 | NEUROLOGIC: Central nervous system > Function > Movement > Spastic quadriplegia | HP:0002510 | T2186 | |
phenodb:1930 | NEUROLOGIC: Central nervous system > Function > Movement > Spasticity | HP:0001257 | T2255 | |
phenodb:1931 | NEUROLOGIC: Central nervous system > Function > Movement > Startle response, exaggerated | HP:0002267 | T2163 | |
phenodb:1932 | NEUROLOGIC: Central nervous system > Function > Movement > Stroke-like episodes | HP:0002401 | T2170 | |
phenodb:1933 | NEUROLOGIC: Central nervous system > Function > Movement > Transient ischemic attack(s) | HP:0002326 | T2169 | |
phenodb:1934 | NEUROLOGIC: Central nervous system > Function > Movement > Tremor | HP:0001337 | T2205 | |
phenodb:1935 | NEUROLOGIC: Central nervous system > Function > Movement > Tremor > Intention | HP:0002080 | T2208 | |
phenodb:1936 | NEUROLOGIC: Central nervous system > Function > Movement > Tremor > Postural | HP:0002174 | T2207 | |
phenodb:1937 | NEUROLOGIC: Central nervous system > Function > Movement > Tremor > Resting | HP:0002322 | T2206 | |
phenodb:1938 | NEUROLOGIC: Central nervous system > Function > Movement > Tremor > Other feature | |||
phenodb:3677 | NEUROLOGIC: Central nervous system > Function > Movement > Upper limb spasticity | HP:0006986 | T2250 | |
phenodb:1939 | NEUROLOGIC: Central nervous system > Function > Movement > Vertigo | HP:0002321 | T0705 | |
phenodb:3408 | NEUROLOGIC: Central nervous system > Function > Movement > Vocal tic | HP:0100035 | T2223 | |
phenodb:1940 | NEUROLOGIC: Central nervous system > Function > Movement > Writer's cramp | HP:0002356 | T2213 | |
phenodb:2897 | NEUROLOGIC: Central nervous system > Function > Movement > Other feature | |||
phenodb:1941 | NEUROLOGIC: Central nervous system > Function > Reflexes | |||
phenodb:1942 | NEUROLOGIC: Central nervous system > Function > Reflexes > Areflexia | HP:0001284 | ||
phenodb:1948 | NEUROLOGIC: Central nervous system > Function > Reflexes > Babinski sign / Extensor plantar response | HP:0003487 | T2246 | |
phenodb:1943 | NEUROLOGIC: Central nervous system > Function > Reflexes > Clonus | HP:0002169 | T2219 | |
phenodb:1944 | NEUROLOGIC: Central nervous system > Function > Reflexes > Clonus > Ankle | HP:0011449 | ||
phenodb:1945 | NEUROLOGIC: Central nervous system > Function > Reflexes > Clonus > Other feature | |||
phenodb:1946 | NEUROLOGIC: Central nervous system > Function > Reflexes > Hyperreflexia | HP:0001347 | T2254 | |
phenodb:1947 | NEUROLOGIC: Central nervous system > Function > Reflexes > Hyporeflexia | HP:0001265 | ||
phenodb:2898 | NEUROLOGIC: Central nervous system > Function > Reflexes > Other feature | |||
phenodb:1949 | NEUROLOGIC: Central nervous system > Function > Seizures / Epilepsy | HP:0001250 | T2259 | |
phenodb:1950 | NEUROLOGIC: Central nervous system > Function > Seizures / Epilepsy > Abnormal EEG | HP:0002353 | T2175 | |
phenodb:1951 | NEUROLOGIC: Central nervous system > Function > Seizures / Epilepsy > Cataplexy | HP:0002524 | ||
phenodb:1952 | NEUROLOGIC: Central nervous system > Function > Seizures / Epilepsy > Hypsarrhythmia | HP:0002521 | ||
phenodb:1953 | NEUROLOGIC: Central nervous system > Function > Seizures / Epilepsy > Infantile spasms | HP:0011097 | ||
phenodb:1954 | NEUROLOGIC: Central nervous system > Function > Seizures / Epilepsy > Normal interictal EEG | HP:0002372 | T2178 | |
phenodb:3409 | NEUROLOGIC: Central nervous system > Function > Seizures / Epilepsy > Seizure | |||
phenodb:1955 | NEUROLOGIC: Central nervous system > Function > Seizures / Epilepsy > Seizures, absence | HP:0002121 | ||
phenodb:1959 | NEUROLOGIC: Central nervous system > Function > Seizures / Epilepsy > Seizures, atonic (drop attacks) | HP:0010819 | ||
phenodb:1958 | NEUROLOGIC: Central nervous system > Function > Seizures / Epilepsy > Seizures, complex | |||
phenodb:1956 | NEUROLOGIC: Central nervous system > Function > Seizures / Epilepsy > Seizures, febrile | HP:0002373 | T2264 | |
phenodb:1957 | NEUROLOGIC: Central nervous system > Function > Seizures / Epilepsy > Seizures, generalized tonic-clonic | HP:0002069 | T2268 | |
phenodb:1960 | NEUROLOGIC: Central nervous system > Function > Seizures / Epilepsy > Seizures, hypoglycemic | HP:0002173 | T2267 | |
phenodb:1961 | NEUROLOGIC: Central nervous system > Function > Seizures / Epilepsy > Seizures, myoclonic | HP:0002123 | T2271 | |
phenodb:1963 | NEUROLOGIC: Central nervous system > Function > Seizures / Epilepsy > Seizures, partial complex | HP:0002384 | T2266 | |
phenodb:1962 | NEUROLOGIC: Central nervous system > Function > Seizures / Epilepsy > Seizures, partial, afebrile | HP:0007359 | T2269 | |
phenodb:1964 | NEUROLOGIC: Central nervous system > Function > Seizures / Epilepsy > Seizures, refractory or intractable | HP:0001250 | ||
phenodb:1965 | NEUROLOGIC: Central nervous system > Function > Seizures / Epilepsy > Status epilepticus | HP:0002133 | T2260 | |
phenodb:1966 | NEUROLOGIC: Central nervous system > Function > Seizures / Epilepsy > Other feature | |||
phenodb:1967 | NEUROLOGIC: Peripheral nervous system | HP:0000759 | ||
phenodb:1968 | NEUROLOGIC: Peripheral nervous system > Structure | |||
phenodb:1970 | NEUROLOGIC: Peripheral nervous system > Structure > Axonal atrophy on nerve biopsy | HP:0003384 | ||
phenodb:1971 | NEUROLOGIC: Peripheral nervous system > Structure > Demyelination | HP:0011096 | T2162 | |
phenodb:1972 | NEUROLOGIC: Peripheral nervous system > Structure > Hypertrophic nerve changes | HP:0003382 | ||
phenodb:3410 | NEUROLOGIC: Peripheral nervous system > Structure > Hypomyelination | HP:0007182 | T2423 | |
phenodb:1973 | NEUROLOGIC: Peripheral nervous system > Structure > Loss of large myelinated fibers | HP:0003387 | ||
phenodb:1969 | NEUROLOGIC: Peripheral nervous system > Structure > 'Onion bulb' formations on nerve biopsy | HP:0003400 | ||
phenodb:1974 | NEUROLOGIC: Peripheral nervous system > Structure > Other feature | |||
phenodb:1975 | NEUROLOGIC: Peripheral nervous system > Function | |||
phenodb:3411 | NEUROLOGIC: Peripheral nervous system > Function > Abnormality of peripheral nerve conduction | HP:0003134 | T2172 | |
phenodb:3412 | NEUROLOGIC: Peripheral nervous system > Function > Abnormality of sometosensory evoked potentials | HP:0007377 | T2173 | |
phenodb:3413 | NEUROLOGIC: Peripheral nervous system > Function > Aphasia | HP:0002381 | T2294 | |
phenodb:1977 | NEUROLOGIC: Peripheral nervous system > Function > Areflexia | HP:0001284 | T2253 | |
phenodb:1978 | NEUROLOGIC: Peripheral nervous system > Function > Axonal degeneration | HP:0000764 | ||
phenodb:1979 | NEUROLOGIC: Peripheral nervous system > Function > Axonal neuropathy | HP:0003477 | ||
phenodb:1980 | NEUROLOGIC: Peripheral nervous system > Function > Decreased miniature end plate potentials | HP:0003402 | ||
phenodb:1981 | NEUROLOGIC: Peripheral nervous system > Function > Decreased nerve conduction velocity | HP:0000762 | T2174 | |
phenodb:1982 | NEUROLOGIC: Peripheral nervous system > Function > Decreased proprioception | HP:0010831 | T2273 | |
phenodb:1983 | NEUROLOGIC: Peripheral nervous system > Function > Decreased vibration sense | HP:0002495 | T2274 | |
phenodb:1984 | NEUROLOGIC: Peripheral nervous system > Function > Distal limb muscle weakness due to peripheral neuropathy | HP:0002460 | ||
phenodb:1985 | NEUROLOGIC: Peripheral nervous system > Function > Distal sensory impairment | HP:0002936 | ||
phenodb:1986 | NEUROLOGIC: Peripheral nervous system > Function > Foot drop | HP:0009027 | T2188 | |
phenodb:3416 | NEUROLOGIC: Peripheral nervous system > Function > Hyperesthesia | HP:0100963 | T2281 | |
phenodb:3414 | NEUROLOGIC: Peripheral nervous system > Function > Hypoesthesia | HP:0003474 | T2278 | |
phenodb:1987 | NEUROLOGIC: Peripheral nervous system > Function > Hyporeflexia | HP:0001265 | T2922 | |
phenodb:1989 | NEUROLOGIC: Peripheral nervous system > Function > Pain insensitivity | HP:0007021 | T2277 | |
phenodb:1990 | NEUROLOGIC: Peripheral nervous system > Function > Paresthesias | HP:0003401 | T2279 | |
phenodb:1991 | NEUROLOGIC: Peripheral nervous system > Function > Peripheral neuropathy | HP:0009830 | T2161 | |
phenodb:1992 | NEUROLOGIC: Peripheral nervous system > Function > Sensory neuropathy | HP:0000763 | T2276 | |
phenodb:3415 | NEUROLOGIC: Peripheral nervous system > Function > Spontaneous sensation of pain | HP:0010833 | ||
phenodb:1976 | NEUROLOGIC: Peripheral nervous system > Function > 'Steppage' gait | HP:0003376 | T2197 | |
phenodb:1993 | NEUROLOGIC: Peripheral nervous system > Function > Other feature | |||
phenodb:1994 | NEUROPSYCHIATRIC: | |||
phenodb:1995 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development | |||
phenodb:3417 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Absent speech | HP:0001344 | T2296 | |
phenodb:3418 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Amnesia | HP:0002354 | T2332 | |
phenodb:1996 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Cognitive decline | HP:0001268 | T2331 | |
phenodb:1997 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Cognitive impairment, mild | HP:0100543 | ||
phenodb:1998 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Developmental delay | HP:0001263 | ||
phenodb:1999 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Developmental delay > Global / Generalized | HP:0001263 | T2312 | |
phenodb:3419 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Developmental delay > Global / Generalized > Mild | HP:0011342 | T2324 | |
phenodb:3420 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Developmental delay > Global / Generalized > Moderate | HP:0011343 | T2325 | |
phenodb:3421 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Developmental delay > Global / Generalized > Severe | HP:0011344 | T2326 | |
phenodb:3422 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Developmental delay > Global / Generalized > Profound | HP:0012736 | T2327 | |
phenodb:3624 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Developmental delay > Global / Generalized > Other feature | |||
phenodb:2000 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Developmental delay > Language | HP:0000750 | ||
phenodb:2001 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Developmental delay > Expressive language (speech) | HP:0002474 | T2298 | |
phenodb:2002 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Developmental delay > Receptive language | HP:0010863 | T2297 | |
phenodb:3423 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Developmental delay > Motor | HP:0001270 | T2309 | |
phenodb:2003 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Developmental delay > Gross motor | HP:0002194 | T2322 | |
phenodb:2004 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Developmental delay > Fine motor | HP:0010862 | T2320 | |
phenodb:2005 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Developmental delay > Other feature | |||
phenodb:2006 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Language development normal | |||
phenodb:2007 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Mental retardation (aka Intellectual disablility / Psychomotor retardation) | HP:0001249 | T2310 | |
phenodb:3424 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Mental retardation (aka Intellectual disablility / Psychomotor retardation) > Borderline (IQ 70-85) | HP:0006889 | ||
phenodb:2008 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Mental retardation (aka Intellectual disablility / Psychomotor retardation) > Mild (IQ 50-70) | HP:0001256 | T2317 | |
phenodb:2009 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Mental retardation (aka Intellectual disablility / Psychomotor retardation) > Moderate (IQ 35-50) | HP:0002342 | T2316 | |
phenodb:2011 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Mental retardation (aka Intellectual disablility / Psychomotor retardation) > Severe (IQ 20-35) | HP:0010864 | T2314 | |
phenodb:2010 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Mental retardation (aka Intellectual disablility / Psychomotor retardation) > Profound (IQ below 20) | HP:0002187 | T2315 | |
phenodb:2012 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Mental retardation (aka Intellectual disablility / Psychomotor retardation) > Other feature | |||
phenodb:2013 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Learning disabilities | HP:0001328 | T2308 | |
phenodb:3425 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Learning disabilities > Agraphia | |||
phenodb:3426 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Learning disabilities > Alexia | HP:0010523 | T2306 | |
phenodb:2015 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Learning disabilities > Dysgraphia | HP:0010526 | T2923 | |
phenodb:2014 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Learning disabilities > Dyslexia | HP:0010522 | T2307 | |
phenodb:2016 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Learning disabilities > Other feature | |||
phenodb:2017 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Dementia | HP:0000726 | T2328 | |
phenodb:2018 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Developmental regression / Loss of milestones / Neurodegeneration | HP:0002376 | T2330 | |
phenodb:2899 | NEUROPSYCHIATRIC: Cognition / Intelligence / Development > Other feature | |||
phenodb:2019 | NEUROPSYCHIATRIC: Behavior | HP:0000708 | ||
phenodb:2020 | NEUROPSYCHIATRIC: Behavior > Aggressive behavior | HP:0000718 | T2372 | |
phenodb:2021 | NEUROPSYCHIATRIC: Behavior > Agitation | HP:0000713 | T2346 | |
phenodb:2022 | NEUROPSYCHIATRIC: Behavior > Apathy | HP:0000741 | T2364 | |
phenodb:2023 | NEUROPSYCHIATRIC: Behavior > Autistic features | HP:0000729 | ||
phenodb:2024 | NEUROPSYCHIATRIC: Behavior > Autistic features > Poor eye contact | HP:0000817 | T2319 | |
phenodb:2025 | NEUROPSYCHIATRIC: Behavior > Autistic features > Poor peer or social relationships | HP:0000728 | T2353 | |
phenodb:2026 | NEUROPSYCHIATRIC: Behavior > Autistic features > Repetitive or stereotypical behavior | HP:0000733 | ||
phenodb:3427 | NEUROPSYCHIATRIC: Behavior > Autistic features > Restricted behavior | HP:0000723 | T2354 | |
phenodb:2027 | NEUROPSYCHIATRIC: Behavior > Autistic features > Other feature | |||
phenodb:2028 | NEUROPSYCHIATRIC: Behavior > Behavioral changes | HP:0000708 | ||
phenodb:2029 | NEUROPSYCHIATRIC: Behavior > Behavioral problems | HP:0000708 | ||
phenodb:3428 | NEUROPSYCHIATRIC: Behavior > Echolalia | HP:0010529 | T2293 | |
phenodb:3678 | NEUROPSYCHIATRIC: Behavior > Fatigue | HP:0012378 | T2866 | |
phenodb:2030 | NEUROPSYCHIATRIC: Behavior > Happy demeanor | HP:0100024 | T2344 | |
phenodb:2031 | NEUROPSYCHIATRIC: Behavior > Hyperactivity | HP:0000752 | ||
phenodb:2032 | NEUROPSYCHIATRIC: Behavior > Hyperorality | HP:0000710 | T2342 | |
phenodb:2033 | NEUROPSYCHIATRIC: Behavior > Hyperphagia | HP:0002591 | T2360 | |
phenodb:2034 | NEUROPSYCHIATRIC: Behavior > Impulsivity | HP:0100710 | T2347 | |
phenodb:2035 | NEUROPSYCHIATRIC: Behavior > Inattention / Attention deficit | HP:0000736 | T2333 | |
phenodb:2036 | NEUROPSYCHIATRIC: Behavior > Irritability | HP:0000737 | T2363 | |
phenodb:2037 | NEUROPSYCHIATRIC: Behavior > Perseveration / Perseverative behavior | HP:0000733 | ||
phenodb:2038 | NEUROPSYCHIATRIC: Behavior > Personality changes | HP:0000751 | T2345 | |
phenodb:2039 | NEUROPSYCHIATRIC: Behavior > Restlessness | HP:0000711 | ||
phenodb:2040 | NEUROPSYCHIATRIC: Behavior > Self-injurious behavior | HP:0100716 | T2371 | |
phenodb:2041 | NEUROPSYCHIATRIC: Behavior > Stereotyped, repetitive behavior | HP:0000733 | T2225 | |
phenodb:3429 | NEUROPSYCHIATRIC: Behavior > Stuttering | |||
phenodb:2900 | NEUROPSYCHIATRIC: Behavior > Other feature | |||
phenodb:2042 | NEUROPSYCHIATRIC: Psychiatric Illness | HP:0000708 | ||
phenodb:3430 | NEUROPSYCHIATRIC: Psychiatric Illness > Anorexia nervosa | |||
phenodb:2043 | NEUROPSYCHIATRIC: Psychiatric Illness > Anxiety | HP:0000739 | T2361 | |
phenodb:2044 | NEUROPSYCHIATRIC: Psychiatric Illness > Attention deficit hyperactivity disorder | HP:0007018 | T2335 | |
phenodb:2045 | NEUROPSYCHIATRIC: Psychiatric Illness > Autism | HP:0000717 | ||
phenodb:2046 | NEUROPSYCHIATRIC: Psychiatric Illness > Bipolar disorder | HP:0007302 | ||
phenodb:3431 | NEUROPSYCHIATRIC: Psychiatric Illness > Bulimia | HP:0100739 | T2359 | |
phenodb:2047 | NEUROPSYCHIATRIC: Psychiatric Illness > Delusions | HP:0000746 | T2343 | |
phenodb:2048 | NEUROPSYCHIATRIC: Psychiatric Illness > Depression | HP:0000716 | T2362 | |
phenodb:2049 | NEUROPSYCHIATRIC: Psychiatric Illness > Disinhibition | HP:0000734 | T2351 | |
phenodb:2050 | NEUROPSYCHIATRIC: Psychiatric Illness > Emotional lability | HP:0000712 | T2164 | |
phenodb:2051 | NEUROPSYCHIATRIC: Psychiatric Illness > Frontal release signs | HP:0000743 | ||
phenodb:2052 | NEUROPSYCHIATRIC: Psychiatric Illness > Hallucinations | HP:0000738 | T2357 | |
phenodb:2053 | NEUROPSYCHIATRIC: Psychiatric Illness > Mania | HP:0100754 | T2370 | |
phenodb:2054 | NEUROPSYCHIATRIC: Psychiatric Illness > Mood swings | HP:0000720 | T2165 | |
phenodb:2055 | NEUROPSYCHIATRIC: Psychiatric Illness > Mutism | HP:0002300 | T2292 | |
phenodb:2056 | NEUROPSYCHIATRIC: Psychiatric Illness > Obsessive-compulsive disorder | HP:0000722 | T2356 | |
phenodb:2057 | NEUROPSYCHIATRIC: Psychiatric Illness > Psychosis | HP:0000709 | T2367 | |
phenodb:2058 | NEUROPSYCHIATRIC: Psychiatric Illness > Schizophrenia | HP:0100753 | ||
phenodb:2059 | NEUROPSYCHIATRIC: Psychiatric Illness > Other feature | |||
phenodb:2060 | SKIN, NAILS, HAIR: | |||
phenodb:2061 | SKIN, NAILS, HAIR: Skin | HP:0000951 | ||
phenodb:2062 | SKIN, NAILS, HAIR: Skin > General abnormalities | HP:0000951 | T1196 | |
phenodb:2063 | SKIN, NAILS, HAIR: Skin > General abnormalities > Acne | HP:0001061 | T1272 | |
phenodb:2064 | SKIN, NAILS, HAIR: Skin > General abnormalities > Atopic dermatitis | HP:0001047 | T1245 | |
phenodb:3687 | SKIN, NAILS, HAIR: Skin > General abnormalities > Atrophodermia vermiculata | HP:0100837 | T1263 | |
phenodb:3432 | SKIN, NAILS, HAIR: Skin > General abnormalities > Cellulitis | HP:0100658 | T1220 | |
phenodb:2065 | SKIN, NAILS, HAIR: Skin > General abnormalities > Cigarette-paper scars | HP:0001073 | T1228 | |
phenodb:3442 | SKIN, NAILS, HAIR: Skin > General abnormalities > Cutis marmorata | HP:0000965 | T1242 | |
phenodb:3433 | SKIN, NAILS, HAIR: Skin > General abnormalities > Dermatitis | HP:0011123 | T1278 | |
phenodb:3436 | SKIN, NAILS, HAIR: Skin > General abnormalities > Dimple | HP:0010781 | T1234 | |
phenodb:2066 | SKIN, NAILS, HAIR: Skin > General abnormalities > Dry skin | HP:0000958 | ||
phenodb:2067 | SKIN, NAILS, HAIR: Skin > General abnormalities > Erysipelas | HP:0001055 | T1250 | |
phenodb:3447 | SKIN, NAILS, HAIR: Skin > General abnormalities > Erythema | HP:0010783 | T1249 | |
phenodb:3446 | SKIN, NAILS, HAIR: Skin > General abnormalities > Erythroderma | HP:0001019 | T1248 | |
phenodb:3679 | SKIN, NAILS, HAIR: Skin > General abnormalities > Facial angiofibroma | HP:0009720 | ||
phenodb:3434 | SKIN, NAILS, HAIR: Skin > General abnormalities > Hypoplastic | |||
phenodb:3448 | SKIN, NAILS, HAIR: Skin > General abnormalities > Macule | HP:0012733 | T1251 | |
phenodb:3449 | SKIN, NAILS, HAIR: Skin > General abnormalities > Papule | HP:0200034 | T1253 | |
phenodb:3438 | SKIN, NAILS, HAIR: Skin > General abnormalities > Peeling | |||
phenodb:3437 | SKIN, NAILS, HAIR: Skin > General abnormalities > Pit | HP:0100276 | T1235 | |
phenodb:2068 | SKIN, NAILS, HAIR: Skin > General abnormalities > Pruritus | HP:0000989 | T1265 | |
phenodb:3445 | SKIN, NAILS, HAIR: Skin > General abnormalities > Psoriasis | HP:0003765 | ||
phenodb:3444 | SKIN, NAILS, HAIR: Skin > General abnormalities > Rash | HP:0000988 | T1244 | |
phenodb:3439 | SKIN, NAILS, HAIR: Skin > General abnormalities > Scaly | |||
phenodb:3435 | SKIN, NAILS, HAIR: Skin > General abnormalities > Seborrhea | HP:0001051 | T1214 | |
phenodb:3441 | SKIN, NAILS, HAIR: Skin > General abnormalities > Skin infection | HP:0001581 | ||
phenodb:3443 | SKIN, NAILS, HAIR: Skin > General abnormalities > Skin photosensitivity | HP:0000992 | T1243 | |
phenodb:3440 | SKIN, NAILS, HAIR: Skin > General abnormalities > Skin ulcers | HP:0200042 | T1240 | |
phenodb:2069 | SKIN, NAILS, HAIR: Skin > General abnormalities > Urticaria | HP:0001025 | T1246 | |
phenodb:2070 | SKIN, NAILS, HAIR: Skin > General abnormalities > Xerosis | HP:0000958 | T1208 | |
phenodb:2071 | SKIN, NAILS, HAIR: Skin > General abnormalities > Other feature | |||
phenodb:2072 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities | HP:0001000 | T1279 | |
phenodb:2073 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Acanthosis nigricans | HP:0000956 | ||
phenodb:2077 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Acrocyanosis | HP:0001063 | T1823 | |
phenodb:2074 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Albinism | HP:0001022 | T1284 | |
phenodb:2075 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Axillary freckling | HP:0000997 | T1297 | |
phenodb:2076 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Cafe-au-lait spots | HP:0000957 | T1294 | |
phenodb:2078 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Fair skin (aka Diffuse hypopigmentation) | HP:0007513 | T1282 | |
phenodb:2079 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Freckling | HP:0001480 | T1298 | |
phenodb:2080 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Hyperpigmentation | HP:0000953 | T1286 | |
phenodb:3450 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Hyperpigmented skin patches | HP:0007400 | T1287 | |
phenodb:2081 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Hypopigmented skin patches | HP:0001053 | T1285 | |
phenodb:2082 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Inguinal freckling | HP:0030052 | ||
phenodb:2083 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Jaundice | HP:0000952 | T1540 | |
phenodb:2084 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Lentigines | HP:0001003 | T1290 | |
phenodb:3453 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Linear nevus | HP:0010817 | T1291 | |
phenodb:3452 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Melanocytic nevus | HP:0003764 | ||
phenodb:3454 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Mongolian spot | HP:0100814 | T1295 | |
phenodb:2085 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Nevus flammeus | HP:0001052 | T1302 | |
phenodb:3457 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Pallor | HP:0000980 | T2867 | |
phenodb:2086 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Petechiae | HP:0000967 | T1307 | |
phenodb:2087 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Pigmented nevi | HP:0000995 | T1289 | |
phenodb:3455 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Poikiloderma | HP:0001029 | T1313 | |
phenodb:2088 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Purpura | HP:0000979 | T1308 | |
phenodb:3451 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Reticular hyperpigmentation | HP:0007588 | T1288 | |
phenodb:2089 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Rosacea | |||
phenodb:3456 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Shagreen patch | HP:0009721 | T1232 | |
phenodb:2090 | SKIN, NAILS, HAIR: Skin > Pigmentary abnormalities > Other feature | |||
phenodb:2091 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies | HP:0000951 | ||
phenodb:2092 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > General | HP:0000951 | ||
phenodb:3460 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > General > Abnormal scar formation | HP:0000987 | T1226 | |
phenodb:2093 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > General > Atrophy | HP:0007488 | T1215 | |
phenodb:2094 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > General > Blistering, generalized | HP:0008066 | T1254 | |
phenodb:2095 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > General > Blistering, recurrent | HP:0008066 | ||
phenodb:3462 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > General > Bulla | |||
phenodb:2097 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > General > Doughy | HP:0001027 | ||
phenodb:2096 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > General > Erosions | HP:0200041 | T1268 | |
phenodb:2098 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > General > Fragility | HP:0001030 | T1267 | |
phenodb:3465 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > General > Furuncles, recurrent | HP:0011132 | ||
phenodb:3461 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > General > Hairy patch | |||
phenodb:2099 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > General > Laxity (aka Cutis laxa, Loose skin, Redundant skin) | HP:0000973 | T1277 | |
phenodb:3459 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > General > Palmoplantar pustulosis | HP:0100847 | T1225 | |
phenodb:2107 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > General > Poor wound healing | HP:0001058 | T1229 | |
phenodb:3464 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > General > Pustule | HP:0200039 | T1260 | |
phenodb:3458 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > General > Scleroderma | HP:0100324 | T1206 | |
phenodb:2100 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > General > Soft | HP:0000977 | ||
phenodb:2101 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > General > Stiff | HP:0030053 | ||
phenodb:2102 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > General > Thick | HP:0001072 | T1271 | |
phenodb:2103 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > General > Thin | HP:0000963 | T1266 | |
phenodb:2104 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > General > Translucent | HP:0010648 | T1207 | |
phenodb:2105 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > General > Velvety | HP:0000977 | T1197 | |
phenodb:3463 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > General > Vesicle | HP:0200037 | T1256 | |
phenodb:2106 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > General > Wrinkled | HP:0100678 | T1233 | |
phenodb:2108 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > General > Other feature | |||
phenodb:2109 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Epidermis | HP:0011124 | ||
phenodb:2110 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Epidermis > Acanthosis | HP:0000956 | T1293 | |
phenodb:2111 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Epidermis > Cutis aplasia | HP:0001057 | T1218 | |
phenodb:2112 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Epidermis > Eczema | HP:0000964 | ||
phenodb:2113 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Epidermis > Epidermal hyperplasia | HP:0011368 | ||
phenodb:2114 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Epidermis > Epidermolysis bullosa, dystrophic | |||
phenodb:2115 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Epidermis > Epidermolysis bullosa, simplex | |||
phenodb:2116 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Epidermis > Hyperextensible skin | HP:0000974 | T1276 | |
phenodb:2117 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Epidermis > Hyperkeratosis | HP:0000962 | T1221 | |
phenodb:2118 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Epidermis > Ichthyosis | HP:0008064 | T1239 | |
phenodb:2119 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Epidermis > Keloids | HP:0010562 | T1227 | |
phenodb:2120 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Epidermis > Keratosis pilaris | HP:0007468 | ||
phenodb:2121 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Epidermis > Palmoplantar hyperkeratosis | HP:0000972 | ||
phenodb:2122 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Epidermis > Palmoplantar keratoderma | HP:0000982 | T1224 | |
phenodb:2126 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Epidermis > Perifollicular fibrosis | HP:0030054 | ||
phenodb:2127 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Epidermis > Perifollicular inflammation | HP:0012322 | ||
phenodb:2123 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Epidermis > Sacral dimple | HP:0000960 | T0865 | |
phenodb:2124 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Epidermis > Scars, atrophic | HP:0001075 | T1230 | |
phenodb:2125 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Epidermis > Striae | HP:0001065 | T1219 | |
phenodb:2128 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Epidermis > Other feature | |||
phenodb:2129 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Dermis | |||
phenodb:2130 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Dermis > Anhidrosis | HP:0000970 | T1213 | |
phenodb:2131 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Dermis > Follicular hyperkeratosis | HP:0007502 | T1223 | |
phenodb:2132 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Dermis > Hyperhidrosis | HP:0000975 | T1209 | |
phenodb:2133 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Dermis > Hypohidrosis | HP:0000966 | T1212 | |
phenodb:2134 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Dermis > Milia | HP:0001056 | T1204 | |
phenodb:2135 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Dermis > Other feature | |||
phenodb:2136 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Vascular / Lymphatic | HP:0011276 | T1299 | |
phenodb:2137 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Vascular / Lymphatic > Angiokeratoma | HP:0001014 | T1315 | |
phenodb:2138 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Vascular / Lymphatic > Easy bruising | HP:0000978 | T1834 | |
phenodb:2139 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Vascular / Lymphatic > Hemangiomas | HP:0001028 | T1300 | |
phenodb:3466 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Vascular / Lymphatic > Hemangiomas > Cavernous | HP:0001048 | T1303 | |
phenodb:3467 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Vascular / Lymphatic > Hemangiomas > Capillary | HP:0005306 | T1304 | |
phenodb:3468 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Vascular / Lymphatic > Hemangiomas > Facial | HP:0000329 | T1305 | |
phenodb:3625 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Vascular / Lymphatic > Hemangiomas > Other feature | |||
phenodb:2140 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Vascular / Lymphatic > Lymphedema | HP:0001004 | T1849 | |
phenodb:2141 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Vascular / Lymphatic > Prominent veins | HP:0007457 | ||
phenodb:2142 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Vascular / Lymphatic > Telangiectasia | HP:0001009 | T1310 | |
phenodb:2143 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Vascular / Lymphatic > Other feature | |||
phenodb:2144 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Growths | HP:0008069 | T1314 | |
phenodb:2145 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Growths > Lipoma | HP:0012032 | T1319 | |
phenodb:2146 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Growths > Neurofibromas | HP:0100698 | T1322 | |
phenodb:3469 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Growths > Papilloma | HP:0012740 | T1318 | |
phenodb:3470 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Growths > Skin tag | HP:0010609 | T1325 | |
phenodb:3471 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Growths > Subcutaneous nodule | HP:0001482 | T1324 | |
phenodb:3472 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Growths > Wart | HP:0200043 | T1317 | |
phenodb:2147 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Growths > Xanthoma | HP:0001114 | T1320 | |
phenodb:2148 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Growths > Other feature | |||
phenodb:2149 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Electron microscopy | |||
phenodb:2150 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Electron microscopy > Cleavage within basal keratinocytes | |||
phenodb:2151 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Electron microscopy > Decreased staining for collagen VII | |||
phenodb:2152 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Electron microscopy > Hypotrophic anchoring fibrils | |||
phenodb:2153 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Electron microscopy > Sublamina densa level of tissue separation beneath basal membrane | |||
phenodb:2154 | SKIN, NAILS, HAIR: Skin > Structural defects, anomalies > Electron microscopy > Other feature | |||
phenodb:2155 | SKIN, NAILS, HAIR: Nails | HP:0001597 | T1371 | |
phenodb:3473 | SKIN, NAILS, HAIR: Nails > Anomaly | |||
phenodb:3474 | SKIN, NAILS, HAIR: Nails > Anomaly > Fingers | HP:0001231 | T1393 | |
phenodb:2156 | SKIN, NAILS, HAIR: Nails > Absent | HP:0001798 | T1379 | |
phenodb:3475 | SKIN, NAILS, HAIR: Nails > Absent > Toes | HP:0008388 | T1400 | |
phenodb:2157 | SKIN, NAILS, HAIR: Nails > Absent > Fingers | HP:0001817 | T1396 | |
phenodb:2158 | SKIN, NAILS, HAIR: Nails > Absent > Toes | HP:0001802 | T1404 | |
phenodb:3476 | SKIN, NAILS, HAIR: Nails > Bifid | HP:0010793 | T1385 | |
phenodb:3477 | SKIN, NAILS, HAIR: Nails > Broad | HP:0001821 | T1386 | |
phenodb:2160 | SKIN, NAILS, HAIR: Nails > Brittle | HP:0001808 | ||
phenodb:2161 | SKIN, NAILS, HAIR: Nails > Brittle > Fingers | |||
phenodb:2162 | SKIN, NAILS, HAIR: Nails > Brittle > Toes | |||
phenodb:3481 | SKIN, NAILS, HAIR: Nails > Color | |||
phenodb:3482 | SKIN, NAILS, HAIR: Nails > Color > Leukonychia | HP:0001820 | T1407 | |
phenodb:3483 | SKIN, NAILS, HAIR: Nails > Color > Melanonychia | HP:0100644 | T1408 | |
phenodb:3478 | SKIN, NAILS, HAIR: Nails > Concave | HP:0001598 | T1387 | |
phenodb:2164 | SKIN, NAILS, HAIR: Nails > Dysplastic | HP:0002164 | ||
phenodb:2165 | SKIN, NAILS, HAIR: Nails > Dysplastic > Fingers | |||
phenodb:2166 | SKIN, NAILS, HAIR: Nails > Dysplastic > Toes | HP:0100797 | T1402 | |
phenodb:2168 | SKIN, NAILS, HAIR: Nails > Dystrophic | HP:0008404 | T1375 | |
phenodb:2169 | SKIN, NAILS, HAIR: Nails > Dystrophic > Fingers | HP:0008391 | T1398 | |
phenodb:2170 | SKIN, NAILS, HAIR: Nails > Dystrophic > Toes | HP:0001810 | T1403 | |
phenodb:2172 | SKIN, NAILS, HAIR: Nails > Hyperconvex | HP:0001795 | b06081c45a5ba7a6 | |
phenodb:2173 | SKIN, NAILS, HAIR: Nails > Hyperconvex > Fingers | HP:0001812 | T1378 | |
phenodb:2174 | SKIN, NAILS, HAIR: Nails > Hyperconvex > Toes | HP:0030055 | ||
phenodb:2176 | SKIN, NAILS, HAIR: Nails > Hypoplastic | HP:0001792 | 164fef3895cda7aa | |
phenodb:2177 | SKIN, NAILS, HAIR: Nails > Hypoplastic > Fingers | HP:0001804 | T1395 | |
phenodb:3479 | SKIN, NAILS, HAIR: Nails > Hypoplastic > Fingers > Hypoplastic fifth fingernail | HP:0008398 | T2913 | |
phenodb:2178 | SKIN, NAILS, HAIR: Nails > Hypoplastic > Toes | HP:0001800 | T1401 | |
phenodb:2180 | SKIN, NAILS, HAIR: Nails > Longitudinal ridging | HP:0001807 | ||
phenodb:2181 | SKIN, NAILS, HAIR: Nails > Longitudinal ridging > Fingers | |||
phenodb:2182 | SKIN, NAILS, HAIR: Nails > Longitudinal ridging > Toes | |||
phenodb:2184 | SKIN, NAILS, HAIR: Nails > Onycholysis | HP:0001806 | T1409 | |
phenodb:2185 | SKIN, NAILS, HAIR: Nails > Onycholysis > Fingers | HP:0008400 | T1394 | |
phenodb:2186 | SKIN, NAILS, HAIR: Nails > Onycholysis > Toes | |||
phenodb:3480 | SKIN, NAILS, HAIR: Nails > Periungual fibroma | HP:0100804 | T1392 | |
phenodb:2188 | SKIN, NAILS, HAIR: Nails > Pitted | HP:0001803 | T1411 | a7e46325a44dd469 |
phenodb:2189 | SKIN, NAILS, HAIR: Nails > Pitted > Fingers | |||
phenodb:2190 | SKIN, NAILS, HAIR: Nails > Pitted > Toes | |||
phenodb:2192 | SKIN, NAILS, HAIR: Nails > Paronychia | HP:0001818 | T1405 | 90a6f3c1605fb539 |
phenodb:2193 | SKIN, NAILS, HAIR: Nails > Paronychia > Fingers | |||
phenodb:2194 | SKIN, NAILS, HAIR: Nails > Paronychia > Toes | |||
phenodb:2196 | SKIN, NAILS, HAIR: Nails > Ridged | HP:0001807 | T1388 | a1e42d67c7465887 |
phenodb:2197 | SKIN, NAILS, HAIR: Nails > Ridged > Fingers | |||
phenodb:2198 | SKIN, NAILS, HAIR: Nails > Ridged > Toes | |||
phenodb:2200 | SKIN, NAILS, HAIR: Nails > Short | HP:0001799 | T1377 | 2f191de8ba67fa81 |
phenodb:2201 | SKIN, NAILS, HAIR: Nails > Short > Fingers | HP:0001821 | ||
phenodb:2202 | SKIN, NAILS, HAIR: Nails > Short > Toes | |||
phenodb:2204 | SKIN, NAILS, HAIR: Nails > Thick | HP:0001805 | T1376 | |
phenodb:2205 | SKIN, NAILS, HAIR: Nails > Thick > Fingers | |||
phenodb:2206 | SKIN, NAILS, HAIR: Nails > Thick > Toes | |||
phenodb:2208 | SKIN, NAILS, HAIR: Nails > Thin | HP:0001816 | T1380 | 5418a886448cff2d |
phenodb:2209 | SKIN, NAILS, HAIR: Nails > Thin > Fingers | HP:0012742 | T1381 | |
phenodb:2210 | SKIN, NAILS, HAIR: Nails > Thin > Toes | |||
phenodb:2901 | SKIN, NAILS, HAIR: Nails > Other feature | |||
phenodb:2212 | SKIN, NAILS, HAIR: Hair | HP:0001595 | ||
phenodb:2213 | SKIN, NAILS, HAIR: Hair > General | HP:0001595 | ||
phenodb:3484 | SKIN, NAILS, HAIR: Hair > General > Alopecia areata | HP:0002229 | T1338 | |
phenodb:3485 | SKIN, NAILS, HAIR: Hair > General > Alopecia universalis | HP:0002289 | T1340 | |
phenodb:3486 | SKIN, NAILS, HAIR: Hair > General > Hypopigmentation of the hair | HP:0005599 | T1342 | |
phenodb:2214 | SKIN, NAILS, HAIR: Hair > General > Pili canaliculi | HP:0002235 | T1351 | |
phenodb:2215 | SKIN, NAILS, HAIR: Hair > General > Pili tortii (aka twisted hair shaft) | HP:0003777 | ||
phenodb:2216 | SKIN, NAILS, HAIR: Hair > General > Trichorrhexis nodosa | HP:0009886 | T1358 | |
phenodb:2218 | SKIN, NAILS, HAIR: Hair > General > Uncombable hair | HP:0030056 | ||
phenodb:2219 | SKIN, NAILS, HAIR: Hair > General > Wooly hair | HP:0002224 | ||
phenodb:2220 | SKIN, NAILS, HAIR: Hair > General > Other feature | |||
phenodb:2221 | SKIN, NAILS, HAIR: Hair > Head | |||
phenodb:2222 | SKIN, NAILS, HAIR: Hair > Facial | |||
phenodb:2224 | SKIN, NAILS, HAIR: Hair > Facial > Eyebrows | HP:0000534 | ||
phenodb:2225 | SKIN, NAILS, HAIR: Hair > Facial > Eyelashes | HP:0000499 | ||
phenodb:2226 | SKIN, NAILS, HAIR: Hair > Facial > Facial hypertrichosis | HP:0002219 | T1329 | |
phenodb:2223 | SKIN, NAILS, HAIR: Hair > Facial > Hairline | HP:0009553 | ||
phenodb:2902 | SKIN, NAILS, HAIR: Hair > Facial > Other feature | |||
phenodb:2227 | SKIN, NAILS, HAIR: Hair > Body | |||
phenodb:2228 | SKIN, NAILS, HAIR: Hair > Body > Alopecia, totalis | HP:0007418 | T1339 | |
phenodb:2229 | SKIN, NAILS, HAIR: Hair > Body > Axillary hair | HP:0100134 | ||
phenodb:2230 | SKIN, NAILS, HAIR: Hair > Body > Axillary hair > Absent | HP:0002221 | ||
phenodb:2231 | SKIN, NAILS, HAIR: Hair > Body > Axillary hair > Sparse | HP:0002215 | T1335 | |
phenodb:2232 | SKIN, NAILS, HAIR: Hair > Body > Axillary hair > Other feature | |||
phenodb:2233 | SKIN, NAILS, HAIR: Hair > Body > Hypertrichosis / Hirsutism | HP:0000998 | T1327 | |
phenodb:3487 | SKIN, NAILS, HAIR: Hair > Body > Localized hypertrichosis | |||
phenodb:2234 | SKIN, NAILS, HAIR: Hair > Body > Hypotrichosis | HP:0001006 | ||
phenodb:2235 | SKIN, NAILS, HAIR: Hair > Body > Pubic hair | HP:0100133 | ||
phenodb:2236 | SKIN, NAILS, HAIR: Hair > Body > Pubic hair > Absent | HP:0002555 | ||
phenodb:2237 | SKIN, NAILS, HAIR: Hair > Body > Pubic hair > Sparse | HP:0002225 | T1334 | |
phenodb:2238 | SKIN, NAILS, HAIR: Hair > Body > Pubic hair > Other feature | |||
phenodb:2239 | SKIN, NAILS, HAIR: Hair > Body > Sparse hair | HP:0008070 | T1331 | |
phenodb:2903 | SKIN, NAILS, HAIR: Hair > Body > Other feature | |||
phenodb:2240 | IMMUNOLOGY: | HP:0002715 | T2524 | |
phenodb:2241 | IMMUNOLOGY: Agammaglobulinemia | HP:0004432 | T2536 | |
phenodb:2854 | IMMUNOLOGY: Allergies | |||
phenodb:2855 | IMMUNOLOGY: Allergies > Food | |||
phenodb:2856 | IMMUNOLOGY: Allergies > Food > Specify | |||
phenodb:2858 | IMMUNOLOGY: Allergies > Food > Specify | |||
phenodb:2857 | IMMUNOLOGY: Allergies > Drug | |||
phenodb:2859 | IMMUNOLOGY: Allergies > Venom | |||
phenodb:2911 | IMMUNOLOGY: Allergies > Specify | |||
phenodb:2904 | IMMUNOLOGY: Allergies > Other feature | |||
phenodb:3680 | IMMUNOLOGY: Angioedema | HP:0100665 | T2872 | |
phenodb:2242 | IMMUNOLOGY: Antibodies, deficient, NOS | |||
phenodb:2243 | IMMUNOLOGY: Autoimmune antibodies | HP:0030057 | ||
phenodb:2244 | IMMUNOLOGY: Autoimmune antibodies > Antinuclear antibody positive | HP:0003493 | ||
phenodb:2246 | IMMUNOLOGY: Autoimmune antibodies > Neutrophil antibody positive | HP:0003453 | ||
phenodb:2247 | IMMUNOLOGY: Autoimmune antibodies > Phospholipid antibody positive | HP:0003613 | ||
phenodb:2248 | IMMUNOLOGY: Autoimmune antibodies > Platelet antibody positive | HP:0003454 | ||
phenodb:2249 | IMMUNOLOGY: Autoimmune antibodies > Rheumatoid factor positive | HP:0002923 | ||
phenodb:2250 | IMMUNOLOGY: Autoimmune antibodies > Smooth muscle antibody positive | HP:0003262 | ||
phenodb:2245 | IMMUNOLOGY: Autoimmune antibodies > Other, specify | |||
phenodb:2251 | IMMUNOLOGY: Autoimmune disorders | HP:0002960 | T2543 | |
phenodb:2252 | IMMUNOLOGY: Autoimmune disorders > Specify | |||
phenodb:2860 | IMMUNOLOGY: B cell deficiency | HP:0010976 | T2535 | |
phenodb:2253 | IMMUNOLOGY: Complement deficiency | HP:0004431 | T2541 | |
phenodb:2254 | IMMUNOLOGY: Complement deficiency > Specify | HP:0004431 | ||
phenodb:2255 | IMMUNOLOGY: C-reactive protein, increased | HP:0011227 | T2870 | |
phenodb:2256 | IMMUNOLOGY: Erythrocyte sedimentation rate (ESR), increased | HP:0003565 | T2871 | |
phenodb:3488 | IMMUNOLOGY: Abnormal immunoglobulin level | HP:0010701 | T2526 | |
phenodb:2257 | IMMUNOLOGY: Hypogammaglobulinemia | HP:0004313 | T2537 | |
phenodb:2258 | IMMUNOLOGY: IgA deficiency | HP:0002720 | T2532 | |
phenodb:2259 | IMMUNOLOGY: IgE increased | HP:0003212 | T2525 | |
phenodb:2260 | IMMUNOLOGY: IgM deficiency | HP:0002850 | T2531 | |
phenodb:3489 | IMMUNOLOGY: IgG increased | HP:0003237 | T2542 | |
phenodb:3490 | IMMUNOLOGY: Humoral immune deficiency | |||
phenodb:3491 | IMMUNOLOGY: Cellular immune deficiency | HP:0005374 | T2539 | |
phenodb:2861 | IMMUNOLOGY: Immunodeficiency, combined variable (aka CVID, or combined variable immunodeficiency) | HP:0005387 | ||
phenodb:2862 | IMMUNOLOGY: Immunodeficiency, disorder of innate immunity | |||
phenodb:2863 | IMMUNOLOGY: Immunodeficiency, severe combined (aka SCID, or severe combined immunodeficiency) | HP:0004430 | T2538 | |
phenodb:2261 | IMMUNOLOGY: Immunodeficiency, NOS | HP:0002721 | T2527 | |
phenodb:3492 | IMMUNOLOGY: Immune hypersensitivity | HP:0100326 | T2544 | |
phenodb:2262 | IMMUNOLOGY: Infection, opportunistic | HP:0005390 | T2530 | |
phenodb:2263 | IMMUNOLOGY: Infection, opportunistic > Specify pathogen | |||
phenodb:2264 | IMMUNOLOGY: Infections, recurrent | HP:0002719 | T2528 | |
phenodb:2265 | IMMUNOLOGY: Infections, recurrent > Bacterial | HP:0002718 | T2533 | |
phenodb:2912 | IMMUNOLOGY: Infections, recurrent > Bacterial > Specify pathogen | |||
phenodb:2266 | IMMUNOLOGY: Infections, recurrent > Fungal | HP:0002841 | T2534 | |
phenodb:2913 | IMMUNOLOGY: Infections, recurrent > Fungal > Specify pathogen | |||
phenodb:2267 | IMMUNOLOGY: Infections, recurrent > Viral | HP:0004429 | T2529 | |
phenodb:2914 | IMMUNOLOGY: Infections, recurrent > Viral > Specify pathogen | |||
phenodb:2268 | IMMUNOLOGY: Infections, recurrent > Other pathogen | |||
phenodb:2269 | IMMUNOLOGY: Lymphadenopathy | HP:0002716 | T1844 | |
phenodb:2270 | IMMUNOLOGY: Lymphopenia | HP:0001888 | ||
phenodb:3493 | IMMUNOLOGY: Mastocytosis | HP:0100495 | T2810 | |
phenodb:2271 | IMMUNOLOGY: Neutropenia | HP:0001875 | ||
phenodb:2272 | IMMUNOLOGY: Nitroblue tetrazolium (NBT) reduction test, negative | HP:0003203 | ||
phenodb:2864 | IMMUNOLOGY: NK cell deficiency | |||
phenodb:3494 | IMMUNOLOGY: Sepsis | HP:0100806 | T2869 | |
phenodb:2273 | IMMUNOLOGY: T cell, absent or deficient | HP:0005379 | T2540 | |
phenodb:2274 | IMMUNOLOGY: T cell, absent or deficient > Specify subtype, if known | |||
phenodb:2275 | IMMUNOLOGY: Thymus hypoplasia (or small or absent) | HP:0000778 | T2920 | |
phenodb:2905 | IMMUNOLOGY: Other feature | |||
phenodb:2276 | ENDOCRINE FEATURES: | HP:0000818 | ||
phenodb:2277 | ENDOCRINE FEATURES: Pituitary | HP:0012503 | T2048 | |
phenodb:3495 | ENDOCRINE FEATURES: Pituitary > Abnormality of the hypothalamus-pituitary axis | HP:0000864 | T2039 | |
phenodb:2278 | ENDOCRINE FEATURES: Pituitary > Acromegaly | HP:0000845 | ||
phenodb:3496 | ENDOCRINE FEATURES: Pituitary > Calcification | HP:0010513 | T2045 | |
phenodb:2279 | ENDOCRINE FEATURES: Pituitary > Cushing syndrome | HP:0001578 | T2070 | |
phenodb:2280 | ENDOCRINE FEATURES: Pituitary > Panhypopituitarism | HP:0000871 | T2044 | |
phenodb:3497 | ENDOCRINE FEATURES: Pituitary > Ectopic anterior pituitary gland | HP:0012731 | T2042 | |
phenodb:2281 | ENDOCRINE FEATURES: Pituitary > Diabetes insipidus, central | HP:0000863 | T2052 | |
phenodb:2282 | ENDOCRINE FEATURES: Pituitary > Galactorrhea | HP:0100829 | T2093 | |
phenodb:2283 | ENDOCRINE FEATURES: Pituitary > Gigantism | HP:0000845 | T2837 | |
phenodb:2284 | ENDOCRINE FEATURES: Pituitary > Growth hormone deficiency | HP:0000824 | T2049 | |
phenodb:3498 | ENDOCRINE FEATURES: Pituitary > Hyperpituitarism | HP:0010514 | T2047 | |
phenodb:2285 | ENDOCRINE FEATURES: Pituitary > Hypogonadotropic hypogonadism | HP:0000044 | T2088 | |
phenodb:2286 | ENDOCRINE FEATURES: Pituitary > Hypothyroidism, tertiary (central) | HP:0011787 | T2040 | |
phenodb:2287 | ENDOCRINE FEATURES: Pituitary > Other feature | |||
phenodb:2288 | ENDOCRINE FEATURES: Thyroid | HP:0000820 | T2053 | |
phenodb:3501 | ENDOCRINE FEATURES: Thyroid > Agenesis | HP:0008191 | T2058 | |
phenodb:3499 | ENDOCRINE FEATURES: Thyroid > Ectopic thyroid | HP:0100028 | T2056 | |
phenodb:2289 | ENDOCRINE FEATURES: Thyroid > Hyperthyroidism | HP:0000836 | T2060 | |
phenodb:3500 | ENDOCRINE FEATURES: Thyroid > Hypoplasia | HP:0005990 | T2057 | |
phenodb:2290 | ENDOCRINE FEATURES: Thyroid > Hypothyroidism | HP:0000821 | T2059 | |
phenodb:3502 | ENDOCRINE FEATURES: Thyroid > Thyroiditis | HP:0100646 | T2061 | |
phenodb:2291 | ENDOCRINE FEATURES: Thyroid > Other feature | |||
phenodb:2292 | ENDOCRINE FEATURES: Parathyroid | HP:0000828 | T2062 | |
phenodb:2293 | ENDOCRINE FEATURES: Parathyroid > Hyperparathyroidism | HP:0000843 | ||
phenodb:2294 | ENDOCRINE FEATURES: Parathyroid > Hypoparathyroidism | HP:0000829 | T2064 | |
phenodb:2295 | ENDOCRINE FEATURES: Parathyroid > Pseudohypoparathyroidism | HP:0000852 | ||
phenodb:2296 | ENDOCRINE FEATURES: Parathyroid > Other feature | |||
phenodb:2297 | ENDOCRINE FEATURES: Pancreas, endocrine | HP:0012093 | ||
phenodb:2298 | ENDOCRINE FEATURES: Pancreas, endocrine > Diabetes mellitus | HP:0000819 | T2074 | |
phenodb:2299 | ENDOCRINE FEATURES: Pancreas, endocrine > Diabetes mellitus > Insulin-resistant | HP:0000831 | T2076 | |
phenodb:2300 | ENDOCRINE FEATURES: Pancreas, endocrine > Diabetes mellitus > Insulin-dependent | HP:0100651 | T2075 | |
phenodb:2301 | ENDOCRINE FEATURES: Pancreas, endocrine > Diabetes mellitus > Other feature | |||
phenodb:2302 | ENDOCRINE FEATURES: Pancreas, endocrine > Hyperinsulinism | HP:0000842 | T2079 | |
phenodb:2303 | ENDOCRINE FEATURES: Pancreas, endocrine > Hyperinsulinism > Neonatal | |||
phenodb:2304 | ENDOCRINE FEATURES: Pancreas, endocrine > Hyperinsulinism > Other feature | |||
phenodb:3503 | ENDOCRINE FEATURES: Pancreas, endocrine > Insulin resistance | HP:0000855 | T2078 | |
phenodb:2305 | ENDOCRINE FEATURES: Pancreas, endocrine > Maturity onset diabetes of the young (MODY) | HP:0004904 | T2077 | |
phenodb:2306 | ENDOCRINE FEATURES: Adrenals | HP:0000834 | T2065 | |
phenodb:3505 | ENDOCRINE FEATURES: Adrenals > Adrenal calcification | HP:0010512 | T2066 | |
phenodb:3504 | ENDOCRINE FEATURES: Adrenals > Adrenal hyperplasia | HP:0008221 | T2069 | |
phenodb:2307 | ENDOCRINE FEATURES: Adrenals > Adrenal hypoplasia | HP:0000835 | T2068 | |
phenodb:2308 | ENDOCRINE FEATURES: Adrenals > Adrenal insufficiency / Addison disease | HP:0000846 | T2067 | |
phenodb:2309 | ENDOCRINE FEATURES: Adrenals > Cushing disease | HP:0001578 | ||
phenodb:2310 | ENDOCRINE FEATURES: Adrenals > Hyperaldosteronism | HP:0000859 | T2071 | |
phenodb:3506 | ENDOCRINE FEATURES: Adrenals > Hypoaldosteronism | HP:0004319 | T2072 | |
phenodb:2311 | ENDOCRINE FEATURES: Adrenals > Pheochromocytoma | HP:0002666 | ||
phenodb:2312 | ENDOCRINE FEATURES: Adrenals > Other feature | |||
phenodb:2313 | ENDOCRINE FEATURES: Puberty / Reproduction-related | |||
phenodb:2314 | ENDOCRINE FEATURES: Puberty / Reproduction-related > Amenorrhea, primay | HP:0000786 | ||
phenodb:2315 | ENDOCRINE FEATURES: Puberty / Reproduction-related > Amenorrhea, secondary | HP:0000869 | T2090 | |
phenodb:2316 | ENDOCRINE FEATURES: Puberty / Reproduction-related > Hyperandrogenism | |||
phenodb:2317 | ENDOCRINE FEATURES: Puberty / Reproduction-related > Hypogonadism | HP:0000135 | T2087 | |
phenodb:2318 | ENDOCRINE FEATURES: Puberty / Reproduction-related > Puberty, delayed | HP:0000823 | T2086 | |
phenodb:2319 | ENDOCRINE FEATURES: Puberty / Reproduction-related > Puberty, precocious | HP:0000826 | T2083 | |
phenodb:3507 | ENDOCRINE FEATURES: Puberty / Reproduction-related > Premature menopause | HP:0100805 | T2089 | |
phenodb:2320 | ENDOCRINE FEATURES: Puberty / Reproduction-related > Other feature | |||
phenodb:2321 | HEMATOLOGY: | HP:0001871 | T2547 | |
phenodb:3508 | HEMATOLOGY: Anomaly of the bone marrow cells | HP:0005561 | T2549 | |
phenodb:2322 | HEMATOLOGY: Anemia | HP:0001903 | T2554 | |
phenodb:2323 | HEMATOLOGY: Anemia > Aplastic | HP:0001915 | T2556 | |
phenodb:2324 | HEMATOLOGY: Anemia > Autoimmune hemolytic | HP:0001890 | T2559 | |
phenodb:2325 | HEMATOLOGY: Anemia > Hemolytic, NOS | HP:0001878 | T2557 | |
phenodb:2326 | HEMATOLOGY: Anemia > Hypochromic | HP:0001931 | T2555 | |
phenodb:2327 | HEMATOLOGY: Anemia > Iron deficiency | HP:0001891 | T2563 | |
phenodb:2328 | HEMATOLOGY: Anemia > Macrocytic | HP:0001972 | T2565 | |
phenodb:2329 | HEMATOLOGY: Anemia > Megaloblastic | HP:0001889 | T2566 | |
phenodb:2330 | HEMATOLOGY: Anemia > Microcytic | HP:0001935 | T2561 | |
phenodb:3509 | HEMATOLOGY: Anemia > Normocytic | HP:0001897 | T2564 | |
phenodb:2331 | HEMATOLOGY: Anemia > Sideroblastic | HP:0001924 | T2560 | |
phenodb:2332 | HEMATOLOGY: Anemia > Other feature | |||
phenodb:3515 | HEMATOLOGY: Basophil abnormality | HP:0001912 | T2577 | |
phenodb:2333 | HEMATOLOGY: Bleeding diathesis / Coagulopathy (See Laboratory, coagulation for specific tests) | HP:0001892 | T2595 | |
phenodb:3514 | HEMATOLOGY: Eosinophil abnormality | HP:0001879 | T2575 | |
phenodb:2334 | HEMATOLOGY: Eosinophilia | HP:0001880 | T2576 | |
phenodb:3510 | HEMATOLOGY: Hemoglobinopathy | HP:0011902 | T2571 | |
phenodb:2335 | HEMATOLOGY: Histiocytes, sea blue | HP:0001982 | T2585 | |
phenodb:3513 | HEMATOLOGY: Leukocyte abnormality | HP:0001881 | T2572 | |
phenodb:2336 | HEMATOLOGY: Leukocytosis | HP:0001974 | T2574 | |
phenodb:2337 | HEMATOLOGY: Leukopenia | HP:0001882 | T2573 | |
phenodb:3517 | HEMATOLOGY: Lymphocyte abnormality | HP:0004332 | T2581 | |
phenodb:2338 | HEMATOLOGY: Lymphocytes, vacuolated | HP:0001922 | T2582 | |
phenodb:2339 | HEMATOLOGY: Lymphopenia | HP:0001888 | T2583 | |
phenodb:2340 | HEMATOLOGY: Lymphocytosis | HP:0100827 | T2584 | |
phenodb:3518 | HEMATOLOGY: Macrophage abnormality | HP:0004311 | T2586 | |
phenodb:2341 | HEMATOLOGY: Myelofibrosis | HP:0011974 | T2808 | |
phenodb:2342 | HEMATOLOGY: Myelodysplasia | HP:0002863 | ||
phenodb:2343 | HEMATOLOGY: Neutropenia | HP:0001875 | T2580 | |
phenodb:3516 | HEMATOLOGY: Neutrophil abnormality | HP:0001874 | T2579 | |
phenodb:3511 | HEMATOLOGY: Neutrophilia | HP:0011897 | T2578 | |
phenodb:2344 | HEMATOLOGY: Pancytopenia | HP:0001876 | T2550 | |
phenodb:3681 | HEMATOLOGY: Platelet abnormality | HP:0001872 | T2587 | |
phenodb:2345 | HEMATOLOGY: Platelet morphology abnormalities | HP:0011875 | T2592 | |
phenodb:2346 | HEMATOLOGY: Platelet morphology abnormalities > Giant | HP:0001902 | T2594 | |
phenodb:2347 | HEMATOLOGY: Platelet morphology abnormalities > Large | HP:0011877 | T2588 | |
phenodb:2348 | HEMATOLOGY: Platelet morphology abnormalities > Small | HP:0005537 | T2593 | |
phenodb:2349 | HEMATOLOGY: Platelet morphology abnormalities > Other feature | |||
phenodb:3512 | HEMATOLOGY: Platelet function abnormality | HP:0011869 | T2591 | |
phenodb:2350 | HEMATOLOGY: Polycythemia | HP:0001901 | T2567 | |
phenodb:2351 | HEMATOLOGY: Red cell morphology abnormalities | HP:0001877 | ||
phenodb:2352 | HEMATOLOGY: Red cell morphology abnormalities > Acanthocytes | HP:0001927 | T1281 | |
phenodb:2353 | HEMATOLOGY: Red cell morphology abnormalities > Schistocytes | HP:0001981 | T2552 | |
phenodb:2354 | HEMATOLOGY: Red cell morphology abnormalities > Sickled cells | HP:0030058 | T2570 | |
phenodb:2355 | HEMATOLOGY: Red cell morphology abnormalities > Other feature | |||
phenodb:2356 | HEMATOLOGY: Reticulocytopenia | HP:0001896 | T2553 | |
phenodb:2357 | HEMATOLOGY: Reticulocytosis | HP:0001923 | T2569 | |
phenodb:2358 | HEMATOLOGY: Thrombocytopenia | HP:0001873 | T2590 | |
phenodb:2359 | HEMATOLOGY: Thrombocytosis | HP:0001894 | T2589 | |
phenodb:2360 | HEMATOLOGY: Thrombophilia (See Laboratory, coagulation for specific tests) | HP:0100724 | T2614 | |
phenodb:2906 | HEMATOLOGY: Other feature | |||
phenodb:2361 | METABOLIC: | |||
phenodb:2362 | METABOLIC: Acidosis | HP:0001941 | T2618 | |
phenodb:2363 | METABOLIC: Acidosis > Hyperchloremic | HP:0001995 | ||
phenodb:2364 | METABOLIC: Acidosis > Ketotic | HP:0001946 | ||
phenodb:2365 | METABOLIC: Acidosis > Organic acid-based | HP:0001942 | ||
phenodb:2366 | METABOLIC: Acidosis > Respiratory | HP:0005972 | ||
phenodb:2367 | METABOLIC: Acidosis > Other feature | |||
phenodb:2368 | METABOLIC: Alkalosis | HP:0001948 | ||
phenodb:2369 | METABOLIC: Alkalosis > Metabolic | HP:0200114 | ||
phenodb:2370 | METABOLIC: Alkalosis > Respiratory | HP:0001950 | ||
phenodb:2371 | METABOLIC: Alkalosis > Other feature | |||
phenodb:2372 | METABOLIC: Dehydration | HP:0001944 | ||
phenodb:2373 | METABOLIC: Fever | HP:0001945 | ||
phenodb:3519 | METABOLIC: Periodic fever | HP:0001954 | ||
phenodb:2374 | METABOLIC: Hyperammonemia | HP:0001987 | T2624 | |
phenodb:2375 | METABOLIC: Hyperglycemia (non-diabetic, see endocrine for diabetes) | HP:0003074 | ||
phenodb:2376 | METABOLIC: Malignant hyperthermia | HP:0002047 | T2868 | |
phenodb:2377 | METABOLIC: Hypoglycemia | HP:0001943 | T2080 | |
phenodb:2378 | METABOLIC: Hypoglycemia > Ketotic | HP:0012734 | T2081 | |
phenodb:2379 | METABOLIC: Hypoglycemia > Non-ketotic | HP:0001958 | T2082 | |
phenodb:2380 | METABOLIC: Hypoglycemia > Other feature | |||
phenodb:2381 | METABOLIC: Ketosis | HP:0001946 | ||
phenodb:2382 | METABOLIC: Lactic acidosis | HP:0003128 | ||
phenodb:2383 | METABOLIC: Mitochondrial dysfunction | HP:0003287 | T2643 | |
phenodb:2384 | METABOLIC: Mitochondrial dysfunction > Mitochondrial depletion | HP:0030059 | ||
phenodb:3520 | METABOLIC: Mitochondrial dysfunction > Mitochondrial respiratory complex deficiency | |||
phenodb:2385 | METABOLIC: Mitochondrial dysfunction > Mitochondrial respiratory complex I deficiency | HP:0011923 | ||
phenodb:2918 | METABOLIC: Mitochondrial dysfunction > Mitochondrial respiratory complex II deficiency | HP:0008314 | ||
phenodb:2386 | METABOLIC: Mitochondrial dysfunction > Mitochondrial respiratory complex III deficiency | HP:0011924 | ||
phenodb:2387 | METABOLIC: Mitochondrial dysfunction > Mitochondrial respiratory complex IV deficiency | HP:0008347 | ||
phenodb:2388 | METABOLIC: Mitochondrial dysfunction > Mitochondrial respiratory complex V | HP:0011925 | ||
phenodb:2389 | METABOLIC: Mitochondrial dysfunction > Other feature | |||
phenodb:2390 | METABOLIC: Polydipsia | HP:0001959 | ||
phenodb:2391 | METABOLIC: Polyuria | HP:0000103 | T1941 | |
phenodb:2907 | METABOLIC: Other feature | |||
phenodb:2392 | NEOPLASIA: | HP:0002664 | T2684 | |
phenodb:2393 | NEOPLASIA: Brain / Central nervous system cancer | HP:0100006 | T2786 | |
phenodb:2394 | NEOPLASIA: Brain / Central nervous system cancer > Astrocytoma | HP:0009592 | T2789 | |
phenodb:2395 | NEOPLASIA: Brain / Central nervous system cancer > Atypical teratoid / Rhabdoid tumor | |||
phenodb:3525 | NEOPLASIA: Brain / Central nervous system cancer > Benign tumor of the central nervous system | HP:0100835 | T2794 | |
phenodb:2520 | NEOPLASIA: Brain / Central nervous system cancer > Chordoma | HP:0010762 | ||
phenodb:2396 | NEOPLASIA: Brain / Central nervous system cancer > Craniopharyngioma | HP:0030062 | ||
phenodb:2397 | NEOPLASIA: Brain / Central nervous system cancer > Ependymoblastoma | HP:0030066 | ||
phenodb:2398 | NEOPLASIA: Brain / Central nervous system cancer > Ependymoma | HP:0002888 | ||
phenodb:2399 | NEOPLASIA: Brain / Central nervous system cancer > Esthesioneuroblastoma (aka Olfactory nerve tumor) | HP:0030068 | ||
phenodb:2400 | NEOPLASIA: Brain / Central nervous system cancer > Ganglioneuroma | HP:0003005 | ||
phenodb:2401 | NEOPLASIA: Brain / Central nervous system cancer > Germ cell tumor | HP:0100312 | ||
phenodb:3521 | NEOPLASIA: Brain / Central nervous system cancer > Glial cell tumor | |||
phenodb:3522 | NEOPLASIA: Brain / Central nervous system cancer > Glioblastoma | HP:0100843 | T2929 | |
phenodb:2402 | NEOPLASIA: Brain / Central nervous system cancer > Glioma | HP:0009733 | T2790 | |
phenodb:2403 | NEOPLASIA: Brain / Central nervous system cancer > Lymphoma, primary CNS | HP:0030069 | ||
phenodb:2404 | NEOPLASIA: Brain / Central nervous system cancer > Medulloblastoma | HP:0002885 | T2792 | |
phenodb:2405 | NEOPLASIA: Brain / Central nervous system cancer > Medulloepithelioma | HP:0030071 | ||
phenodb:2406 | NEOPLASIA: Brain / Central nervous system cancer > Meningioma | HP:0002858 | T2793 | |
phenodb:2407 | NEOPLASIA: Brain / Central nervous system cancer > Neuroblastoma | HP:0003006 | T2791 | |
phenodb:2408 | NEOPLASIA: Brain / Central nervous system cancer > Paraganglioma | HP:0002668 | T2765 | |
phenodb:2409 | NEOPLASIA: Brain / Central nervous system cancer > Pineal parenchymal tumor | HP:0010799 | ||
phenodb:2410 | NEOPLASIA: Brain / Central nervous system cancer > Pituitary adenoma | HP:0002893 | T2043 | |
phenodb:2411 | NEOPLASIA: Brain / Central nervous system cancer > Primitive neuroectodermal tumor (PNET), Supratentorial (pineoblastoma included) | HP:0030070 | ||
phenodb:2412 | NEOPLASIA: Brain / Central nervous system cancer > Schwannoma | HP:0100008 | T2788 | |
phenodb:3523 | NEOPLASIA: Brain / Central nervous system cancer > Tumor of the pituitary gland | |||
phenodb:3524 | NEOPLASIA: Brain / Central nervous system cancer > Tumor of the spinal cord | HP:0010302 | T2787 | |
phenodb:2413 | NEOPLASIA: Brain / Central nervous system cancer > Tympanic nerve tumors | HP:0006715 | ||
phenodb:2414 | NEOPLASIA: Brain / Central nervous system cancer > Vagal nerve tumors | HP:0002886 | ||
phenodb:2415 | NEOPLASIA: Brain / Central nervous system cancer > Vestibular schwannoma | HP:0009588 | T0694 | |
phenodb:2416 | NEOPLASIA: Brain / Central nervous system cancer > Other feature | |||
phenodb:2417 | NEOPLASIA: Head and neck | HP:0001288 | ||
phenodb:2418 | NEOPLASIA: Head and neck > Eye | HP:0100012 | T2769 | |
phenodb:2419 | NEOPLASIA: Head and neck > Eye > Intraocular melanoma | HP:0007716 | T2773 | |
phenodb:2420 | NEOPLASIA: Head and neck > Eye > Retinoblastoma | HP:0009919 | T2770 | |
phenodb:2421 | NEOPLASIA: Head and neck > Eye > Other feature | |||
phenodb:2422 | NEOPLASIA: Head and neck > Oral | HP:0100649 | ||
phenodb:2423 | NEOPLASIA: Head and neck > Oral > Lip Tumor | HP:0100604 | T2700 | |
phenodb:2424 | NEOPLASIA: Head and neck > Oral > Salivary gland cancer | HP:0100684 | ||
phenodb:2425 | NEOPLASIA: Head and neck > Oral > Other feature | |||
phenodb:2426 | NEOPLASIA: Head and neck > Nasopharyngeal | HP:0100630 | T2690 | |
phenodb:3538 | NEOPLASIA: Head and neck > Nasopharyngeal > Benign tumor of the salivary glands | |||
phenodb:3540 | NEOPLASIA: Head and neck > Nasopharyngeal > Odontogenic benign tumor | |||
phenodb:3541 | NEOPLASIA: Head and neck > Nasopharyngeal > Odontogenic malignant tumor | |||
phenodb:2428 | NEOPLASIA: Head and neck > Nasopharyngeal > Oral cavity cancer | |||
phenodb:3539 | NEOPLASIA: Head and neck > Nasopharyngeal > Tongue tumor | HP:0100648 | T2695 | |
phenodb:3536 | NEOPLASIA: Head and neck > Nasopharyngeal > Tumor of the oropharynx | |||
phenodb:3537 | NEOPLASIA: Head and neck > Nasopharyngeal > Tumor of the salivary glands | HP:0100684 | T2693 | |
phenodb:3542 | NEOPLASIA: Head and neck > Nasopharyngeal > Benign tumor of the nose | |||
phenodb:2427 | NEOPLASIA: Head and neck > Nasopharyngeal > Laryngeal cancer | HP:0012118 | ||
phenodb:3543 | NEOPLASIA: Head and neck > Nasopharyngeal > Malignant tumor of the nose | HP:0012720 | T2687 | |
phenodb:2429 | NEOPLASIA: Head and neck > Nasopharyngeal > Nasal cavity (paranasal sinus cancer) | HP:0030072 | ||
phenodb:2430 | NEOPLASIA: Head and neck > Nasopharyngeal > Pharyngeal | HP:0100638 | ||
phenodb:2431 | NEOPLASIA: Head and neck > Nasopharyngeal > Throat cancer (aka Hypopharyngeal) | |||
phenodb:3544 | NEOPLASIA: Head and neck > Nasopharyngeal > Tumor of the nose | HP:0012720 | T2688 | |
phenodb:2432 | NEOPLASIA: Head and neck > Nasopharyngeal > Other feature | |||
phenodb:2433 | NEOPLASIA: Head and neck > Neck | |||
phenodb:2434 | NEOPLASIA: Head and neck > Neck > Carotid body tumors (chemodectomas) | HP:0030074 | ||
phenodb:2436 | NEOPLASIA: Head and neck > Neck > Parathyroid cancer | HP:0006780 | T2762 | |
phenodb:2435 | NEOPLASIA: Head and neck > Neck > Squamous cell cancer | HP:0002860 | T2775 | |
phenodb:3545 | NEOPLASIA: Head and neck > Neck > Tumor of the parathyroid | HP:0100733 | T2761 | |
phenodb:3546 | NEOPLASIA: Head and neck > Neck > Tumor of the trachea | HP:0100551 | T2722 | |
phenodb:2437 | NEOPLASIA: Head and neck > Neck > Other feature | |||
phenodb:2438 | NEOPLASIA: Chest | |||
phenodb:2439 | NEOPLASIA: Chest > Bronchial tumors | HP:0100522 | ||
phenodb:2440 | NEOPLASIA: Chest > Breast cancer | HP:0003002 | T2731 | |
phenodb:2441 | NEOPLASIA: Chest > Breast cancer > Ductal carcinoma in situ | HP:0030075 | ||
phenodb:2442 | NEOPLASIA: Chest > Breast cancer > Lobular carcinoma in situ | HP:0030076 | ||
phenodb:2443 | NEOPLASIA: Chest > Breast cancer > Male | |||
phenodb:2444 | NEOPLASIA: Chest > Breast cancer > Other feature | |||
phenodb:3547 | NEOPLASIA: Chest > Tumor of the breast | HP:0100013 | T2730 | |
phenodb:2445 | NEOPLASIA: Chest > Heart cancer | |||
phenodb:3548 | NEOPLASIA: Chest > Tumor of the heart | HP:0100544 | T2723 | |
phenodb:2446 | NEOPLASIA: Chest > Lung cancer | HP:0100526 | ||
phenodb:2447 | NEOPLASIA: Chest > Lung cancer > Adenocarcinoma | HP:0030078 | ||
phenodb:2448 | NEOPLASIA: Chest > Lung cancer > Mesothelioma | HP:0100001 | T2771 | |
phenodb:2449 | NEOPLASIA: Chest > Lung cancer > Non-small cell lung cancer | |||
phenodb:2450 | NEOPLASIA: Chest > Lung cancer > Pleuropulmonary blastoma | HP:0100528 | T2727 | |
phenodb:2451 | NEOPLASIA: Chest > Lung cancer > Small cell lung cancer | |||
phenodb:2452 | NEOPLASIA: Chest > Lung cancer > Other feature | |||
phenodb:3549 | NEOPLASIA: Chest > Tumor of the lung | HP:0100526 | T2726 | |
phenodb:2453 | NEOPLASIA: Chest > Thymoma | HP:0100522 | T2728 | |
phenodb:3550 | NEOPLASIA: Chest > Tumor of the thymus | HP:0100521 | T2729 | |
phenodb:2454 | NEOPLASIA: Endocrine | HP:0100568 | T2756 | |
phenodb:2455 | NEOPLASIA: Endocrine > Adrenocortical carcinoma | HP:0006744 | T2767 | |
phenodb:3552 | NEOPLASIA: Endocrine > Adrenomedullary cancer | HP:0100642 | T2766 | |
phenodb:2456 | NEOPLASIA: Endocrine > Islet cell tumors (aka Pancreatic neuroendocrine tumors) | |||
phenodb:2457 | NEOPLASIA: Endocrine > Multiple endocrine neoplasia syndromes | |||
phenodb:2458 | NEOPLASIA: Endocrine > Pheochromocytoma | HP:0002666 | T2764 | |
phenodb:3551 | NEOPLASIA: Endocrine > Tumor of the adrenal gland | HP:0100631 | T2763 | |
phenodb:2459 | NEOPLASIA: Endocrine > Thyroid cancer | HP:0100031 | ||
phenodb:2460 | NEOPLASIA: Endocrine > Thyroid cancer > Anaplastic | HP:0011779 | ||
phenodb:2461 | NEOPLASIA: Endocrine > Thyroid cancer > Follicular | HP:0006731 | ||
phenodb:2462 | NEOPLASIA: Endocrine > Thyroid cancer > Medullary | HP:0002865 | ||
phenodb:2463 | NEOPLASIA: Endocrine > Thyroid cancer > Papillary | HP:0002895 | T2760 | |
phenodb:2464 | NEOPLASIA: Endocrine > Thyroid cancer > Other feature | |||
phenodb:2465 | NEOPLASIA: GI | HP:0007378 | T2703 | |
phenodb:2466 | NEOPLASIA: GI > Appendix cancer | |||
phenodb:3556 | NEOPLASIA: GI > Benign tumor of the esophagus | HP:0100751 | ||
phenodb:2467 | NEOPLASIA: GI > Bile duct cancer, extrahepatic | HP:0100574 | ||
phenodb:2468 | NEOPLASIA: GI > Carcinoid tumor | HP:0100574 | ||
phenodb:2469 | NEOPLASIA: GI > Colon cancer | HP:0003003 | ||
phenodb:2470 | NEOPLASIA: GI > Colorectal cancer | |||
phenodb:2471 | NEOPLASIA: GI > Esophageal cancer | HP:0100751 | T2704 | |
phenodb:2472 | NEOPLASIA: GI > Gallbladder cancer | HP:0100575 | ||
phenodb:2473 | NEOPLASIA: GI > Gastric cancer (aka Stomach cancer) | HP:0012126 | T2708 | |
phenodb:2474 | NEOPLASIA: GI > Gastrointestinal stromal tumors | HP:0100723 | T2784 | |
phenodb:3559 | NEOPLASIA: GI > Hepatoblastoma | HP:0002884 | T2720 | |
phenodb:2475 | NEOPLASIA: GI > Hepatocellular carcinoma (aka Liver cancer) | HP:0001402 | T2719 | |
phenodb:2476 | NEOPLASIA: GI > Pancreatic cancer | HP:0006725 | T2715 | |
phenodb:3562 | NEOPLASIA: GI > Pancreatoblastoma | HP:0100757 | T2717 | |
phenodb:2477 | NEOPLASIA: GI > Rectal cancer | HP:0100833 | ||
phenodb:2478 | NEOPLASIA: GI > Small intestine cancer | HP:0100833 | ||
phenodb:3554 | NEOPLASIA: GI > Tumor of the colon | HP:0100273 | T2711 | |
phenodb:3553 | NEOPLASIA: GI > Tumor of the digestive system | HP:0007378 | T2702 | |
phenodb:3555 | NEOPLASIA: GI > Tumor of the esophagus | HP:0011459 | ||
phenodb:3557 | NEOPLASIA: GI > Tumor of the extrahepatic biliary tract and gallbladder | HP:0100575 | ||
phenodb:3560 | NEOPLASIA: GI > Tumor of the liver | HP:0002896 | T2718 | |
phenodb:3561 | NEOPLASIA: GI > Tumor of the pancreas | HP:0002894 | T2716 | |
phenodb:3563 | NEOPLASIA: GI > Tumor of the rectum | HP:0100743 | T2713 | |
phenodb:3558 | NEOPLASIA: GI > Tumor of the stomach | HP:0006753 | T2707 | |
phenodb:2479 | NEOPLASIA: GI > Other feature | |||
phenodb:2480 | NEOPLASIA: GU | HP:0010787 | ||
phenodb:2481 | NEOPLASIA: GU > Bladder cancer | HP:0002862 | ||
phenodb:3564 | NEOPLASIA: GU > Tumor of the urinary bladder | HP:0009725 | T2753 | |
phenodb:2482 | NEOPLASIA: GU > Cervical cancer | HP:0030079 | ||
phenodb:2483 | NEOPLASIA: GU > Endometrial cancer | HP:0012114 | ||
phenodb:2484 | NEOPLASIA: GU > Gestational trophoblastic tumor (aka choriocarcinoma) | HP:0100768 | ||
phenodb:2485 | NEOPLASIA: GU > Gonadoblastoma | HP:0000150 | ||
phenodb:2486 | NEOPLASIA: GU > Kidney cancer | HP:0009726 | ||
phenodb:2487 | NEOPLASIA: GU > Kidney cancer > Renal cell carcinoma | HP:0005584 | ||
phenodb:2488 | NEOPLASIA: GU > Kidney cancer > Transitional cell cancer (renal pelvis and ureter included) | HP:0006740 | ||
phenodb:2489 | NEOPLASIA: GU > Kidney cancer > Other feature | |||
phenodb:3566 | NEOPLASIA: GU > Tumor of the kidney | HP:0009726 | T2749 | |
phenodb:2490 | NEOPLASIA: GU > Ovarian cancer | HP:0100615 | ||
phenodb:2491 | NEOPLASIA: GU > Ovarian cancer > Epithelial | |||
phenodb:2492 | NEOPLASIA: GU > Ovarian cancer > Germ cell tumor | |||
phenodb:2493 | NEOPLASIA: GU > Ovarian cancer > Low malignant potential tumor | |||
phenodb:2494 | NEOPLASIA: GU > Ovarian cancer > Other feature | |||
phenodb:3567 | NEOPLASIA: GU > Tumor of the ovary | HP:0100615 | T2736 | |
phenodb:2495 | NEOPLASIA: GU > Penile cancer | |||
phenodb:2496 | NEOPLASIA: GU > Prostate cancer | HP:0012125 | T2743 | |
phenodb:3568 | NEOPLASIA: GU > Tumor of the prostate | HP:0100787 | T2742 | |
phenodb:2497 | NEOPLASIA: GU > Testicular cancer | HP:0010788 | ||
phenodb:3569 | NEOPLASIA: GU > Tumor of the testis | HP:0010788 | T2745 | |
phenodb:3570 | NEOPLASIA: GU > Teratoma of the testis | HP:0100616 | T2746 | |
phenodb:3571 | NEOPLASIA: GU > Testicular seminoma | HP:0100617 | T2747 | |
phenodb:3572 | NEOPLASIA: GU > Teratoma | HP:0009792 | T2777 | |
phenodb:2498 | NEOPLASIA: GU > Urethral cancer | |||
phenodb:3573 | NEOPLASIA: GU > Tumor of the urethra | HP:0100517 | T2752 | |
phenodb:2499 | NEOPLASIA: GU > Uterine cancer | HP:0010784 | T2734 | |
phenodb:2500 | NEOPLASIA: GU > Uterine sarcoma | HP:0002891 | T2735 | |
phenodb:3574 | NEOPLASIA: GU > Tumor of the uterus | HP:0100784 | T1782 | |
phenodb:2501 | NEOPLASIA: GU > Vaginal cancer | HP:0100650 | ||
phenodb:3575 | NEOPLASIA: GU > Tumor of the vagina | HP:0100650 | T2739 | |
phenodb:2502 | NEOPLASIA: GU > Vulvar cancer | |||
phenodb:2503 | NEOPLASIA: GU > Wilms tumor | HP:0002667 | T2751 | |
phenodb:3626 | NEOPLASIA: GU > Other feature | |||
phenodb:3576 | NEOPLASIA: Hematologic | |||
phenodb:2504 | NEOPLASIA: Hematologic > Leukemia | HP:0001909 | T2936 | |
phenodb:3577 | NEOPLASIA: Hematologic > Leukemia > Acute leukemia | HP:0002488 | T2802 | |
phenodb:2505 | NEOPLASIA: Hematologic > Leukemia > Acute leukemia > Acute lymphoblastic leukemia (ALL) | HP:0006721 | T2803 | |
phenodb:2506 | NEOPLASIA: Hematologic > Leukemia > Acute leukemia > Acute myeloid leukemia (AML) | HP:0004808 | T2804 | |
phenodb:3627 | NEOPLASIA: Hematologic > Leukemia > Acute leukemia > Other feature | |||
phenodb:3578 | NEOPLASIA: Hematologic > Leukemia > Chronic leukemia | HP:0005558 | T2806 | |
phenodb:2508 | NEOPLASIA: Hematologic > Leukemia > Chronic leukemia > Chronic lymphocytic leukemia (CLL) | HP:0005550 | T2807 | |
phenodb:2509 | NEOPLASIA: Hematologic > Leukemia > Chronic leukemia > Chronic myelogenous leukemia (CML) | HP:0005506 | T2796 | |
phenodb:3628 | NEOPLASIA: Hematologic > Leukemia > Chronic leukemia > Other feature | |||
phenodb:3629 | NEOPLASIA: Hematologic > Leukemia > Other feature | |||
phenodb:3579 | NEOPLASIA: Hematologic > Lymphoma | HP:0002665 | T2797 | |
phenodb:2507 | NEOPLASIA: Hematologic > Lymphoma > Burkitt lymphoma | HP:0030080 | ||
phenodb:2510 | NEOPLASIA: Hematologic > Lymphoma > Hairy cell leukemia | |||
phenodb:2511 | NEOPLASIA: Hematologic > Lymphoma > Histiocytosis, langerhans cell | HP:0100727 | T2811 | |
phenodb:2512 | NEOPLASIA: Hematologic > Lymphoma > Hodgkin lymphoma | HP:0012189 | ||
phenodb:2513 | NEOPLASIA: Hematologic > Lymphoma > Macroglybulinemia, waldenstrom | HP:0005508 | T2799 | |
phenodb:2514 | NEOPLASIA: Hematologic > Lymphoma > Multiple myeloma (aka Plasma cell neoplasm) | HP:0006775 | T2801 | |
phenodb:2515 | NEOPLASIA: Hematologic > Lymphoma > Myelodysplastic syndromes | HP:0002863 | T2809 | |
phenodb:2516 | NEOPLASIA: Hematologic > Lymphoma > Myeloproliferative disorders, chronic | HP:0005547 | T2805 | |
phenodb:2517 | NEOPLASIA: Hematologic > Lymphoma > Non-Hodgkin lymphoma | HP:0012539 | ||
phenodb:2518 | NEOPLASIA: Hematologic > Lymphoma > Other feature | |||
phenodb:2519 | NEOPLASIA: Bone Cancer | |||
phenodb:2521 | NEOPLASIA: Bone Cancer > Fibrous histiocytoma, malignant | |||
phenodb:2522 | NEOPLASIA: Bone Cancer > Osteosarcoma | HP:0002669 | T2927 | |
phenodb:3580 | NEOPLASIA: Bone Cancer > Tumor of the bone | HP:0010622 | T2462 | |
phenodb:2523 | NEOPLASIA: Bone Cancer > Other feature | |||
phenodb:2524 | NEOPLASIA: Soft tissue | |||
phenodb:2525 | NEOPLASIA: Soft tissue > Angiomyolipoma | HP:0006772 | ||
phenodb:2526 | NEOPLASIA: Soft tissue > Leiomyoma | HP:0007620 | ||
phenodb:2527 | NEOPLASIA: Soft tissue > Rhabdomyosarcoma | HP:0002859 | T2781 | |
phenodb:2528 | NEOPLASIA: Soft tissue > Sarcoma | HP:0100242 | T2779 | |
phenodb:2529 | NEOPLASIA: Soft tissue > Sarcoma > Ewing family | HP:0012254 | ||
phenodb:2530 | NEOPLASIA: Soft tissue > Sarcoma > Kaposi | HP:0100726 | T2783 | |
phenodb:3581 | NEOPLASIA: Soft tissue > Sarcoma > Liposarcoma | HP:0012034 | T2934 | |
phenodb:3582 | NEOPLASIA: Soft tissue > Sarcoma > Myosarcoma | |||
phenodb:2531 | NEOPLASIA: Soft tissue > Sarcoma > Soft tissue | |||
phenodb:2532 | NEOPLASIA: Soft tissue > Sarcoma > Other feature | |||
phenodb:2533 | NEOPLASIA: Soft tissue > Skin | HP:0008069 | ||
phenodb:2534 | NEOPLASIA: Soft tissue > Skin > Basal cell carcinoma | HP:0002671 | T2774 | |
phenodb:2535 | NEOPLASIA: Soft tissue > Skin > Cutaneous T-cell lymphoma (aka Mycosis fungoides) | HP:0012192 | ||
phenodb:2536 | NEOPLASIA: Soft tissue > Skin > Melanoma | HP:0002861 | T2772 | |
phenodb:2537 | NEOPLASIA: Soft tissue > Skin > Merkel cell carcinoma | |||
phenodb:2538 | NEOPLASIA: Soft tissue > Skin > Squamous cell carcinoma (aka Non-melanoma) | HP:0002860 | ||
phenodb:3583 | NEOPLASIA: Soft tissue > Skin > Tumor of the nail | HP:0100826 | T1410 | |
phenodb:2539 | NEOPLASIA: Soft tissue > Skin > Other feature | |||
phenodb:2540 | NEOPLASIA: Other | |||
phenodb:2541 | NEOPLASIA: Other > Germ cell tumor (non-CNS) | |||
phenodb:2542 | NEOPLASIA: Other > Midline tract cancer | |||
phenodb:3584 | NEOPLASIA: Other > Neuroendocrine tumor | HP:0100634 | T2768 | |
phenodb:2543 | NEOPLASIA: Other > Other feature | |||
phenodb:2544 | IN UTERO ABNORMALITIES OF THIS PERSON: | |||
phenodb:2545 | IN UTERO ABNORMALITIES OF THIS PERSON: Assisted reproductive technology | |||
phenodb:2546 | IN UTERO ABNORMALITIES OF THIS PERSON: Assisted reproductive technology > In vitro fertilization | |||
phenodb:2547 | IN UTERO ABNORMALITIES OF THIS PERSON: Assisted reproductive technology > Intracytoplasmic sperm injection (ICSI) | |||
phenodb:2548 | IN UTERO ABNORMALITIES OF THIS PERSON: Assisted reproductive technology > Other feature | |||
phenodb:2549 | IN UTERO ABNORMALITIES OF THIS PERSON: Maternal, general | |||
phenodb:2550 | IN UTERO ABNORMALITIES OF THIS PERSON: Maternal, general > Eclampsia | HP:0100601 | T2888 | |
phenodb:2551 | IN UTERO ABNORMALITIES OF THIS PERSON: Maternal, general > Low maternal serum estriol | HP:0008073 | ||
phenodb:2552 | IN UTERO ABNORMALITIES OF THIS PERSON: Maternal, general > Maternal diabetes | HP:0009800 | T2887 | |
phenodb:2553 | IN UTERO ABNORMALITIES OF THIS PERSON: Maternal, general > Maternal hyperphenylalaninemia | HP:0100610 | T2890 | |
phenodb:2556 | IN UTERO ABNORMALITIES OF THIS PERSON: Maternal, general > Maternal hypertension | HP:0008071 | T6016 | |
phenodb:2554 | IN UTERO ABNORMALITIES OF THIS PERSON: Maternal, general > Maternal seizures | HP:0100622 | T2891 | |
phenodb:2555 | IN UTERO ABNORMALITIES OF THIS PERSON: Maternal, general > Maternal virilization | HP:0008072 | ||
phenodb:2557 | IN UTERO ABNORMALITIES OF THIS PERSON: Maternal, general > Preecplampsia | HP:0100602 | T2889 | |
phenodb:2558 | IN UTERO ABNORMALITIES OF THIS PERSON: Maternal, general > Recurrent miscarriage | HP:0200067 | ||
phenodb:2559 | IN UTERO ABNORMALITIES OF THIS PERSON: Maternal, general > Toxemia | HP:0100603 | ||
phenodb:2560 | IN UTERO ABNORMALITIES OF THIS PERSON: Maternal, general > Other feature | |||
phenodb:2561 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures | |||
phenodb:2562 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Alcohol | |||
phenodb:2563 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Chemicals | |||
phenodb:2564 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Chemicals > Specify | |||
phenodb:2565 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Cocaine / LSD / Other | |||
phenodb:2566 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Cocaine / LSD / Other > Specify | |||
phenodb:2567 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Infectious agent | |||
phenodb:2574 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Infectious agent > AIDS | |||
phenodb:2569 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Infectious agent > Cytomegalovirus | |||
phenodb:2572 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Infectious agent > Hepatitis | |||
phenodb:2573 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Infectious agent > Influenza | |||
phenodb:2571 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Infectious agent > Rubella | |||
phenodb:2570 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Infectious agent > Syphilis | |||
phenodb:2568 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Infectious agent > Toxoplasmosis | |||
phenodb:2575 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Infectious agent > Varicella | |||
phenodb:2576 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Infectious agent > Other feature | |||
phenodb:2577 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Ionizing radiation | |||
phenodb:2578 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Medications | |||
phenodb:2579 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Medications > Analgesics | |||
phenodb:2580 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Medications > Analgesics > Specify | |||
phenodb:2581 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Medications > Antibiotics | |||
phenodb:2582 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Medications > Antibiotics > Specify | |||
phenodb:2583 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Medications > Anticoagulants | |||
phenodb:2584 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Medications > Anticoagulants > Specify | |||
phenodb:2585 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Medications > Anticonvulsants | |||
phenodb:2586 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Medications > Anticonvulsants > Specify | |||
phenodb:2587 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Medications > Chemotherapeutics | |||
phenodb:2588 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Medications > Chemotherapeutics > Specify | |||
phenodb:2589 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Medications > Hormones | |||
phenodb:2590 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Medications > Hormones > Specify | |||
phenodb:2591 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Medications > Hypoglycemic agents | |||
phenodb:2592 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Medications > Hypoglycemic agents > Specify | |||
phenodb:2593 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Medications > Insulin | |||
phenodb:2594 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Medications > Insulin > Specify | |||
phenodb:2595 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Medications > Iodine | |||
phenodb:2596 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Medications > Iodine > Specify | |||
phenodb:2597 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Medications > Sedatives | |||
phenodb:2598 | IN UTERO ABNORMALITIES OF THIS PERSON: Antenatal exposures > Medications > Sedatives > Specify | |||
phenodb:2599 | IN UTERO ABNORMALITIES OF THIS PERSON: Fetal, general | |||
phenodb:3585 | IN UTERO ABNORMALITIES OF THIS PERSON: Fetal, general > Amniotic constriction ring (aka amniotic bands) | HP:0009775 | T0944 | |
phenodb:2600 | IN UTERO ABNORMALITIES OF THIS PERSON: Fetal, general > Decreased fetal movement | HP:0001558 | T2879 | |
phenodb:3586 | IN UTERO ABNORMALITIES OF THIS PERSON: Fetal, general > Increased fetal movement | HP:0010519 | T2878 | |
phenodb:2601 | IN UTERO ABNORMALITIES OF THIS PERSON: Fetal, general > Early severe fetal akinesia sequence | HP:0001989 | T0943 | |
phenodb:2602 | IN UTERO ABNORMALITIES OF THIS PERSON: Fetal, general > Fetal acscites | HP:0001791 | ||
phenodb:2603 | IN UTERO ABNORMALITIES OF THIS PERSON: Fetal, general > Fetal cystic hygroma | HP:0010878 | T0734 | |
phenodb:2604 | IN UTERO ABNORMALITIES OF THIS PERSON: Fetal, general > Fetal seizures | |||
phenodb:2605 | IN UTERO ABNORMALITIES OF THIS PERSON: Fetal, general > Hydrops fetalis | HP:0001789 | T2885 | |
phenodb:2606 | IN UTERO ABNORMALITIES OF THIS PERSON: Fetal, general > Hydrops fetalis > Nonimmune | HP:0001790 | T2886 | |
phenodb:2607 | IN UTERO ABNORMALITIES OF THIS PERSON: Fetal, general > Hydrops fetalis > Other feature | |||
phenodb:2608 | IN UTERO ABNORMALITIES OF THIS PERSON: Fetal, general > Increased nuchal translucency | HP:0010880 | T2875 | |
phenodb:2609 | IN UTERO ABNORMALITIES OF THIS PERSON: Fetal, general > Intrauterine growth retardation | HP:0001511 | T2880 | |
phenodb:2908 | IN UTERO ABNORMALITIES OF THIS PERSON: Fetal, general > Other feature | |||
phenodb:2610 | IN UTERO ABNORMALITIES OF THIS PERSON: Amniotic fluid | |||
phenodb:2611 | IN UTERO ABNORMALITIES OF THIS PERSON: Amniotic fluid > Alpha-fetoprotein | |||
phenodb:2612 | IN UTERO ABNORMALITIES OF THIS PERSON: Amniotic fluid > Alpha-fetoprotein > Increased | HP:0006254 | ||
phenodb:2613 | IN UTERO ABNORMALITIES OF THIS PERSON: Amniotic fluid > Alpha-fetoprotein > Decreased | |||
phenodb:2614 | IN UTERO ABNORMALITIES OF THIS PERSON: Amniotic fluid > Alpha-fetoprotein > Other feature | |||
phenodb:2615 | IN UTERO ABNORMALITIES OF THIS PERSON: Amniotic fluid > Polyhydramnios | HP:0001561 | T2877 | |
phenodb:2616 | IN UTERO ABNORMALITIES OF THIS PERSON: Amniotic fluid > Oligohydramnios | HP:0001562 | T2876 | |
phenodb:2909 | IN UTERO ABNORMALITIES OF THIS PERSON: Amniotic fluid > Other feature | |||
phenodb:2617 | IN UTERO ABNORMALITIES OF THIS PERSON: Delivery | |||
phenodb:2618 | IN UTERO ABNORMALITIES OF THIS PERSON: Delivery > Complete breech presentation | HP:0010860 | ||
phenodb:2619 | IN UTERO ABNORMALITIES OF THIS PERSON: Delivery > Frank breech presentation | HP:0010859 | ||
phenodb:2620 | IN UTERO ABNORMALITIES OF THIS PERSON: Delivery > Incomplete breech presentation | HP:0010861 | ||
phenodb:2621 | IN UTERO ABNORMALITIES OF THIS PERSON: Delivery > Intrauterine fetal demise | |||
phenodb:2622 | IN UTERO ABNORMALITIES OF THIS PERSON: Delivery > Premature birth | HP:0001622 | T2881 | |
phenodb:2623 | IN UTERO ABNORMALITIES OF THIS PERSON: Delivery > Premature birth > Weeks | |||
phenodb:2624 | IN UTERO ABNORMALITIES OF THIS PERSON: Delivery > Premature birth following premature rupture of the fetal membranes | HP:0005100 | ||
phenodb:2625 | IN UTERO ABNORMALITIES OF THIS PERSON: Delivery > Stillbirth or death shortly after birth | HP:0003826 | T2850 | |
phenodb:2626 | IN UTERO ABNORMALITIES OF THIS PERSON: Delivery > Spontaneous abortion | HP:0005268 | ||
phenodb:2910 | IN UTERO ABNORMALITIES OF THIS PERSON: Delivery > Other feature | |||
phenodb:2627 | IN UTERO ABNORMALITIES OF THIS PERSON: Placenta | |||
phenodb:2628 | IN UTERO ABNORMALITIES OF THIS PERSON: Placenta > Abruption | HP:0011419 | ||
phenodb:2629 | IN UTERO ABNORMALITIES OF THIS PERSON: Placenta > Acreta | |||
phenodb:2630 | IN UTERO ABNORMALITIES OF THIS PERSON: Placenta > Placental enlargement | HP:0006267 | ||
phenodb:2631 | IN UTERO ABNORMALITIES OF THIS PERSON: Placenta > Previa | |||
phenodb:2632 | IN UTERO ABNORMALITIES OF THIS PERSON: Placenta > Small or abnormal placenta | HP:0006266 | ||
phenodb:2633 | IN UTERO ABNORMALITIES OF THIS PERSON: Placenta > Other feature | |||
phenodb:2634 | IN UTERO ABNORMALITIES OF THIS PERSON: Umbilical cord | HP:0010881 | T0873 | |
phenodb:2635 | IN UTERO ABNORMALITIES OF THIS PERSON: Umbilical cord > Long umbilical cord | HP:0011417 | ||
phenodb:2636 | IN UTERO ABNORMALITIES OF THIS PERSON: Umbilical cord > Single umbilical artery | HP:0001195 | T1784 | |
phenodb:2637 | IN UTERO ABNORMALITIES OF THIS PERSON: Umbilical cord > Short umbilical cord | HP:0001196 | ||
phenodb:2638 | IN UTERO ABNORMALITIES OF THIS PERSON: Umbilical cord > Other feature | |||
phenodb:2639 | KEY LABORATORY ABNORMALITIES: | |||
phenodb:2640 | KEY LABORATORY ABNORMALITIES: In Blood | |||
phenodb:2641 | KEY LABORATORY ABNORMALITIES: In Blood > Amino Acids | HP:0004337 | T2641 | |
phenodb:2642 | KEY LABORATORY ABNORMALITIES: In Blood > Amino Acids > Abnormal analyte(s) | |||
phenodb:2643 | KEY LABORATORY ABNORMALITIES: In Blood > Amino Acids > Abnormal analyte(s) > Please specify and indicate either above or below the reference range or provide a value with units of measure or scan report report under other result: | |||
phenodb:2644 | KEY LABORATORY ABNORMALITIES: In Blood > Bone | |||
phenodb:2645 | KEY LABORATORY ABNORMALITIES: In Blood > Bone > 25-hydroxyvitamin D, decreased | HP:0010881 | ||
phenodb:2646 | KEY LABORATORY ABNORMALITIES: In Blood > Bone > 1,25-dihydroxyvitamin D, decreased | HP:0012052 | ||
phenodb:2647 | KEY LABORATORY ABNORMALITIES: In Blood > Bone > Alkaline phosphatase | |||
phenodb:2648 | KEY LABORATORY ABNORMALITIES: In Blood > Bone > Alkaline phosphatase > Increased (aka Hyperphosphatasia) | HP:0003155 | ||
phenodb:2649 | KEY LABORATORY ABNORMALITIES: In Blood > Bone > Alkaline phosphatase > Decreased (aka Hypophosphatasia] | HP:0003282 | ||
phenodb:2650 | KEY LABORATORY ABNORMALITIES: In Blood > Bone > Calcium | |||
phenodb:2651 | KEY LABORATORY ABNORMALITIES: In Blood > Bone > Calcium > Increased (aka Hypercalcemia) | HP:0003072 | T2632 | |
phenodb:2652 | KEY LABORATORY ABNORMALITIES: In Blood > Bone > Calcium > Decreased (aka Hypocalcemia) | HP:0002901 | T2633 | |
phenodb:2653 | KEY LABORATORY ABNORMALITIES: In Blood > Bone > C-telopeptide, increased (aka C-TX) | |||
phenodb:2654 | KEY LABORATORY ABNORMALITIES: In Blood > Bone > Inorganic pyrophosphate (PPi), increased | HP:0003491 | ||
phenodb:2655 | KEY LABORATORY ABNORMALITIES: In Blood > Bone > Osteocalcin | |||
phenodb:2656 | KEY LABORATORY ABNORMALITIES: In Blood > Bone > Osteocalcin > Increased | |||
phenodb:2657 | KEY LABORATORY ABNORMALITIES: In Blood > Bone > Osteocalcin > Decreased | |||
phenodb:2658 | KEY LABORATORY ABNORMALITIES: In Blood > Bone > Phosphate | |||
phenodb:2659 | KEY LABORATORY ABNORMALITIES: In Blood > Bone > Phosphate > Increased (aka Hyperphosphatemia) | HP:0002905 | T2637 | |
phenodb:2660 | KEY LABORATORY ABNORMALITIES: In Blood > Bone > Phosphate > Decreased (aka Hypophosphatemia) | HP:0002148 | T2636 | |
phenodb:2661 | KEY LABORATORY ABNORMALITIES: In Blood > Electrolytes | |||
phenodb:2662 | KEY LABORATORY ABNORMALITIES: In Blood > Electrolytes > Chloride | |||
phenodb:2663 | KEY LABORATORY ABNORMALITIES: In Blood > Electrolytes > Chloride > Increased (aka Hyperchloremia) | HP:0011423 | ||
phenodb:2664 | KEY LABORATORY ABNORMALITIES: In Blood > Electrolytes > Chloride > Decreased (aka Hypochloremia) | HP:0003113 | ||
phenodb:2665 | KEY LABORATORY ABNORMALITIES: In Blood > Electrolytes > Magnesium | |||
phenodb:2666 | KEY LABORATORY ABNORMALITIES: In Blood > Electrolytes > Magnesium > Increased (aka Hypermagnesemia) | HP:0002918 | T2665 | |
phenodb:2667 | KEY LABORATORY ABNORMALITIES: In Blood > Electrolytes > Magnesium > Decreased (aka Hypomagnesemia) | HP:0002917 | T2667 | |
phenodb:2668 | KEY LABORATORY ABNORMALITIES: In Blood > Electrolytes > Potassium | |||
phenodb:2669 | KEY LABORATORY ABNORMALITIES: In Blood > Electrolytes > Potassium > Increased (aka Hyperkalemia) | HP:0002153 | T2628 | |
phenodb:2670 | KEY LABORATORY ABNORMALITIES: In Blood > Electrolytes > Potassium > Decreased (aka Hypokalemia) | HP:0002900 | T2627 | |
phenodb:3587 | KEY LABORATORY ABNORMALITIES: In Blood > Electrolytes > Potassium > Decreased episodically (aka Episodic hypokalemia) | HP:0012726 | T2626 | |
phenodb:2671 | KEY LABORATORY ABNORMALITIES: In Blood > Electrolytes > Sodium | |||
phenodb:2672 | KEY LABORATORY ABNORMALITIES: In Blood > Electrolytes > Sodium > Increased (aka Hypernatremia) | HP:0003228 | T2620 | |
phenodb:2673 | KEY LABORATORY ABNORMALITIES: In Blood > Electrolytes > Sodium > Decreased (aka Hyponatremia) | HP:0002902 | T2622 | |
phenodb:2674 | KEY LABORATORY ABNORMALITIES: In Blood > Kidney | |||
phenodb:2675 | KEY LABORATORY ABNORMALITIES: In Blood > Kidney > Blood urea nitrogen (BUN), increased | HP:0003138 | ||
phenodb:2676 | KEY LABORATORY ABNORMALITIES: In Blood > Kidney > Creatinine | |||
phenodb:2677 | KEY LABORATORY ABNORMALITIES: In Blood > Kidney > Creatinine > Increased | HP:0003259 | ||
phenodb:2678 | KEY LABORATORY ABNORMALITIES: In Blood > Kidney > Creatinine > Decreased | HP:0012101 | T2410 | |
phenodb:2679 | KEY LABORATORY ABNORMALITIES: In Blood > Lipids | HP:0003119 | T2651 | |
phenodb:2680 | KEY LABORATORY ABNORMALITIES: In Blood > Lipids > Apolipoprotein B | |||
phenodb:2681 | KEY LABORATORY ABNORMALITIES: In Blood > Lipids > Cholesterol synthetic metabolites | HP:0003464 | ||
phenodb:2682 | KEY LABORATORY ABNORMALITIES: In Blood > Lipids > Cholesterol synthetic metabolites > Specify | |||
phenodb:2683 | KEY LABORATORY ABNORMALITIES: In Blood > Lipids > Cholesterol total | |||
phenodb:2684 | KEY LABORATORY ABNORMALITIES: In Blood > Lipids > Cholesterol total > Increased (aka Hypercholesterolemia) | HP:0003124 | T2653 | |
phenodb:2685 | KEY LABORATORY ABNORMALITIES: In Blood > Lipids > Cholesterol total > Decreased | HP:0003146 | T2657 | |
phenodb:2686 | KEY LABORATORY ABNORMALITIES: In Blood > Lipids > HDL cholesterol | |||
phenodb:2687 | KEY LABORATORY ABNORMALITIES: In Blood > Lipids > HDL cholesterol > Increased | HP:0012184 | ||
phenodb:2688 | KEY LABORATORY ABNORMALITIES: In Blood > Lipids > HDL cholesterol > Decreased | HP:0003233 | T2658 | |
phenodb:2689 | KEY LABORATORY ABNORMALITIES: In Blood > Lipids > Hyperlipidemia, NOS | HP:0003077 | T2654 | |
phenodb:2690 | KEY LABORATORY ABNORMALITIES: In Blood > Lipids > Hypobetalipoproteinemia | HP:0003563 | ||
phenodb:2691 | KEY LABORATORY ABNORMALITIES: In Blood > Lipids > IDL, increased | |||
phenodb:2692 | KEY LABORATORY ABNORMALITIES: In Blood > Lipids > LDL, increased | |||
phenodb:2693 | KEY LABORATORY ABNORMALITIES: In Blood > Lipids > Lipoprotein(a) | HP:0010979 | ||
phenodb:2694 | KEY LABORATORY ABNORMALITIES: In Blood > Lipids > Lipoprotein(a) > Increased | HP:0010980 | ||
phenodb:2695 | KEY LABORATORY ABNORMALITIES: In Blood > Lipids > Lipoprotein(a) > Decreased | HP:0010981 | T2652 | |
phenodb:2696 | KEY LABORATORY ABNORMALITIES: In Blood > Lipids > Triglycerides, increased (aka Triglyceridemia) | HP:0002155 | T2656 | |
phenodb:2697 | KEY LABORATORY ABNORMALITIES: In Blood > Lipids > VLDL, increased | HP:0003362 | ||
phenodb:2698 | KEY LABORATORY ABNORMALITIES: In Blood > Lipids > Other, specify | |||
phenodb:2699 | KEY LABORATORY ABNORMALITIES: In Blood > Liver | |||
phenodb:2700 | KEY LABORATORY ABNORMALITIES: In Blood > Liver > Alanine amino transferase, increased (aka ALT, SGPT) | |||
phenodb:2701 | KEY LABORATORY ABNORMALITIES: In Blood > Liver > Alpha fetoprotein, increased (aka AFP) | HP:0006254 | ||
phenodb:2702 | KEY LABORATORY ABNORMALITIES: In Blood > Liver > Aspartate amino transferase, increased (aka AST, SGOT) | |||
phenodb:2703 | KEY LABORATORY ABNORMALITIES: In Blood > Liver > Alkaline phosphatase | |||
phenodb:2704 | KEY LABORATORY ABNORMALITIES: In Blood > Liver > Alkaline phosphatase > Increased (aka Hyperphosphatasia) | HP:0003155 | ||
phenodb:2705 | KEY LABORATORY ABNORMALITIES: In Blood > Liver > Alkaline phosphatase > Decreased (aka Hypophosphatasia) | HP:0003282 | ||
phenodb:2706 | KEY LABORATORY ABNORMALITIES: In Blood > Liver > Alkaline phosphatase > Other feature | |||
phenodb:2707 | KEY LABORATORY ABNORMALITIES: In Blood > Liver > Albumin, decreased (aka Hypoalbuminemia) | HP:0003073 | ||
phenodb:2708 | KEY LABORATORY ABNORMALITIES: In Blood > Liver > Bilirubin, total, increased (aka Hyperbilirubinemia) | HP:0002904 | ||
phenodb:2709 | KEY LABORATORY ABNORMALITIES: In Blood > Liver > Bilirubin, total, increased (aka Hyperbilirubinemia) > Conjugated (aka Direct hyperbilirubinemia) | HP:0002908 | ||
phenodb:2710 | KEY LABORATORY ABNORMALITIES: In Blood > Liver > Bilirubin, total, increased (aka Hyperbilirubinemia) > Unconjugated (aka Indirect hyperbilirubinemia) | HP:0008282 | T1543 | |
phenodb:2711 | KEY LABORATORY ABNORMALITIES: In Blood > Liver > Ferritin, increased | HP:0003281 | T2629 | |
phenodb:2712 | KEY LABORATORY ABNORMALITIES: In Blood > Liver > Gamma-glutamyl transferase, increased (aka GGT) | |||
phenodb:2713 | KEY LABORATORY ABNORMALITIES: In Blood > Liver > Other, specify | |||
phenodb:2714 | KEY LABORATORY ABNORMALITIES: In Blood > Metabolism | |||
phenodb:2715 | KEY LABORATORY ABNORMALITIES: In Blood > Metabolism > Acid phosphatase, increased | HP:0003148 | ||
phenodb:2716 | KEY LABORATORY ABNORMALITIES: In Blood > Metabolism > Acylcarnitine profile, abnormal | HP:0012071 | ||
phenodb:2717 | KEY LABORATORY ABNORMALITIES: In Blood > Metabolism > Acylcarnitine profile, abnormal > Specify | |||
phenodb:2718 | KEY LABORATORY ABNORMALITIES: In Blood > Metabolism > Adenosylcobalamin (AdoCbl), decreased | HP:0003145 | ||
phenodb:2719 | KEY LABORATORY ABNORMALITIES: In Blood > Metabolism > Carnitine, decreased | HP:0003234 | ||
phenodb:2720 | KEY LABORATORY ABNORMALITIES: In Blood > Metabolism > Catecholamines, increased | HP:0003334 | ||
phenodb:2721 | KEY LABORATORY ABNORMALITIES: In Blood > Metabolism > Galactose, increased | HP:0012024 | ||
phenodb:2722 | KEY LABORATORY ABNORMALITIES: In Blood > Metabolism > Lactate, increased | HP:0002151 | T2411 | |
phenodb:2723 | KEY LABORATORY ABNORMALITIES: In Blood > Metabolism > Uric acid, increased (aka Hyperuricemia) | HP:0002149 | T2662 | |
phenodb:2724 | KEY LABORATORY ABNORMALITIES: In Blood > Metabolism > Methylcobalamin (MeCbl), decreased | HP:0003223 | ||
phenodb:2725 | KEY LABORATORY ABNORMALITIES: In Blood > Metabolism > Prostaglandin E2, increased | HP:0003566 | ||
phenodb:2726 | KEY LABORATORY ABNORMALITIES: In Blood > Metabolism > Purine metabolite, abnormal | HP:0004352 | T2661 | |
phenodb:2727 | KEY LABORATORY ABNORMALITIES: In Blood > Metabolism > Purine metabolite, abnormal > Specify | |||
phenodb:2728 | KEY LABORATORY ABNORMALITIES: In Blood > Metabolism > Pyrimidine metabolite, abnormal | HP:0004353 | T2660 | |
phenodb:2729 | KEY LABORATORY ABNORMALITIES: In Blood > Metabolism > Pyrimidine metabolite, abnormal > Specify | |||
phenodb:2730 | KEY LABORATORY ABNORMALITIES: In Blood > Metabolism > Pyruvate - increased | HP:0003542 | ||
phenodb:2731 | KEY LABORATORY ABNORMALITIES: In Blood > Metabolism > Transferrin glycosylation, abnormal | HP:0003160 | ||
phenodb:2732 | KEY LABORATORY ABNORMALITIES: In Blood > Metabolism > Transferrin glycosylation, abnormal > Specify | |||
phenodb:2733 | KEY LABORATORY ABNORMALITIES: In Blood > Metabolism > Other, specify | |||
phenodb:2734 | KEY LABORATORY ABNORMALITIES: In Blood > Muscle | |||
phenodb:2735 | KEY LABORATORY ABNORMALITIES: In Blood > Muscle > Creatine kinase, increased | HP:0003236 | T2408 | |
phenodb:2736 | KEY LABORATORY ABNORMALITIES: In Blood > Muscle > Creatine kinase, increased > mm fraction increased | |||
phenodb:2737 | KEY LABORATORY ABNORMALITIES: In Blood > Muscle > Creatine kinase, increased > mb fraction increased | |||
phenodb:2738 | KEY LABORATORY ABNORMALITIES: In Blood > Muscle > Creatine kinase, increased > bb fraction increased | |||
phenodb:2739 | KEY LABORATORY ABNORMALITIES: In Blood > Muscle > Creatine kinase, increased > Other feature | |||
phenodb:2740 | KEY LABORATORY ABNORMALITIES: In Blood > Thyroid | |||
phenodb:2741 | KEY LABORATORY ABNORMALITIES: In Blood > Thyroid > Calcitonin, increased | HP:0003528 | T2054 | |
phenodb:2742 | KEY LABORATORY ABNORMALITIES: In Blood > Thyroid > T3 | |||
phenodb:2743 | KEY LABORATORY ABNORMALITIES: In Blood > Thyroid > T3 > Increased | HP:0011788 | ||
phenodb:2744 | KEY LABORATORY ABNORMALITIES: In Blood > Thyroid > T3 > Decreased | |||
phenodb:2745 | KEY LABORATORY ABNORMALITIES: In Blood > Thyroid > Free T4 | |||
phenodb:2746 | KEY LABORATORY ABNORMALITIES: In Blood > Thyroid > Free T4 > Increased | HP:0000836 | ||
phenodb:2747 | KEY LABORATORY ABNORMALITIES: In Blood > Thyroid > Free T4 > Decreased | HP:0000821 | ||
phenodb:2748 | KEY LABORATORY ABNORMALITIES: In Blood > Thyroid > TSH | |||
phenodb:2749 | KEY LABORATORY ABNORMALITIES: In Blood > Thyroid > TSH > Increased | HP:0002925 | ||
phenodb:2750 | KEY LABORATORY ABNORMALITIES: In Blood > Thyroid > TSH > Decreased | |||
phenodb:2751 | KEY LABORATORY ABNORMALITIES: In Blood > Coagulation | T2548 | ||
phenodb:2752 | KEY LABORATORY ABNORMALITIES: In Blood > Coagulation > Bleeding time prolonged | HP:0003010 | T2603 | |
phenodb:2753 | KEY LABORATORY ABNORMALITIES: In Blood > Coagulation > Factor V Leiden mutation | HP:0003225 | T2599 | |
phenodb:2754 | KEY LABORATORY ABNORMALITIES: In Blood > Coagulation > Factor deficiency | HP:0003225 | ||
phenodb:2755 | KEY LABORATORY ABNORMALITIES: In Blood > Coagulation > Factor deficiency > Specify | |||
phenodb:2756 | KEY LABORATORY ABNORMALITIES: In Blood > Coagulation > Fibrinogen | HP:0011898 | ||
phenodb:2757 | KEY LABORATORY ABNORMALITIES: In Blood > Coagulation > Fibrinogen > Increased | HP:0011899 | ||
phenodb:2758 | KEY LABORATORY ABNORMALITIES: In Blood > Coagulation > Fibrinogen > Decreased | HP:0011900 | T2598 | |
phenodb:2759 | KEY LABORATORY ABNORMALITIES: In Blood > Coagulation > Protein C deficiency (aka activated protein C, decreased) | HP:0005543 | T2597 | |
phenodb:2760 | KEY LABORATORY ABNORMALITIES: In Blood > Coagulation > Protein S deficiency | HP:0004855 | T2596 | |
phenodb:2761 | KEY LABORATORY ABNORMALITIES: In Blood > Coagulation > PT prolonged | HP:0008151 | ||
phenodb:2762 | KEY LABORATORY ABNORMALITIES: In Blood > Coagulation > PTT prolonged | HP:0003645 | T2600 | |
phenodb:2763 | KEY LABORATORY ABNORMALITIES: In Blood > Coagulation > Von Willebrand deficiency | HP:0008330 | T2601 | |
phenodb:2764 | KEY LABORATORY ABNORMALITIES: In Blood > Metals and Minerals, abnormal | |||
phenodb:2765 | KEY LABORATORY ABNORMALITIES: In Blood > Metals and Minerals, abnormal > Iron, increased | HP:0003452 | T2666 | |
phenodb:2766 | KEY LABORATORY ABNORMALITIES: In Blood > Metals and Minerals, abnormal > Zinc, decreased | |||
phenodb:2767 | KEY LABORATORY ABNORMALITIES: In Blood > Metals and Minerals, abnormal > Other, specify | |||
phenodb:2768 | KEY LABORATORY ABNORMALITIES: In Blood > Vitamin, abnormal | HP:0100508 | T2669 | |
phenodb:2769 | KEY LABORATORY ABNORMALITIES: In Blood > Vitamin, abnormal > Biotin, decreased | |||
phenodb:2770 | KEY LABORATORY ABNORMALITIES: In Blood > Vitamin, abnormal > Folate, decreased | HP:0100507 | T2677 | |
phenodb:2771 | KEY LABORATORY ABNORMALITIES: In Blood > Vitamin, abnormal > Vitamin A, decreased | HP:0004905 | T2670 | |
phenodb:2772 | KEY LABORATORY ABNORMALITIES: In Blood > Vitamin, abnormal > Vitamin B1, decreased (aka Thiamine) | HP:0100503 | T2671 | |
phenodb:2773 | KEY LABORATORY ABNORMALITIES: In Blood > Vitamin, abnormal > Vitamin B2, decreased (aka Riboflavin) | HP:0100504 | T2672 | |
phenodb:2774 | KEY LABORATORY ABNORMALITIES: In Blood > Vitamin, abnormal > Vitamin B3, decreased (aka Niacin) | HP:0100497 | T2673 | |
phenodb:2775 | KEY LABORATORY ABNORMALITIES: In Blood > Vitamin, abnormal > Vitamin B5, decreased (aka Pantothenic acid) | HP:0100505 | T2674 | |
phenodb:2776 | KEY LABORATORY ABNORMALITIES: In Blood > Vitamin, abnormal > Vitamin B6, decreased (aka Pyridoxine) | HP:0008326 | T2675 | |
phenodb:2777 | KEY LABORATORY ABNORMALITIES: In Blood > Vitamin, abnormal > Vitamin B12, decreased | HP:0100502 | T2678 | |
phenodb:2778 | KEY LABORATORY ABNORMALITIES: In Blood > Vitamin, abnormal > Vitamin C, decreased | HP:0100510 | T2679 | |
phenodb:2779 | KEY LABORATORY ABNORMALITIES: In Blood > Vitamin, abnormal > Vitamin D, decreased | HP:0100512 | T2680 | |
phenodb:2780 | KEY LABORATORY ABNORMALITIES: In Blood > Vitamin, abnormal > Vitamin E, decreased | HP:0100513 | T2681 | |
phenodb:2781 | KEY LABORATORY ABNORMALITIES: In Blood > Vitamin, abnormal > Vitamin K, decreased | HP:0011892 | T2682 | |
phenodb:2782 | KEY LABORATORY ABNORMALITIES: In Blood > Vitamin, abnormal > Other, Specify | |||
phenodb:3588 | KEY LABORATORY ABNORMALITIES: In Blood > Telomeres, short | |||
phenodb:2783 | KEY LABORATORY ABNORMALITIES: In Blood > Other serum proteins | |||
phenodb:2784 | KEY LABORATORY ABNORMALITIES: In Blood > Other serum proteins > Ceruloplasmin, low | HP:0010837 | ||
phenodb:3589 | KEY LABORATORY ABNORMALITIES: In Blood > Other serum proteins > Cryoglobulinemia | HP:0100778 | T2545 | |
phenodb:2785 | KEY LABORATORY ABNORMALITIES: In Blood > Other serum proteins > Other, specify | |||
phenodb:2786 | KEY LABORATORY ABNORMALITIES: In Blood > Other serum proteins > Other, specify | |||
phenodb:2787 | KEY LABORATORY ABNORMALITIES: In Blood > Other serum proteins > Other, specify | |||
phenodb:2788 | KEY LABORATORY ABNORMALITIES: In urine | |||
phenodb:3590 | KEY LABORATORY ABNORMALITIES: In urine > Abnormal color | HP:0012086 | T1943 | |
phenodb:3591 | KEY LABORATORY ABNORMALITIES: In urine > Abnormal odor | HP:0012088 | T1944 | |
phenodb:3592 | KEY LABORATORY ABNORMALITIES: In urine > Amino acids | HP:0003355 | T2640 | |
phenodb:3593 | KEY LABORATORY ABNORMALITIES: In urine > Calcium, increased | HP:0002150 | T2634 | |
phenodb:3594 | KEY LABORATORY ABNORMALITIES: In urine > Calcium, decreased | HP:0003127 | T2635 | |
phenodb:2789 | KEY LABORATORY ABNORMALITIES: In urine > Dicarboxylic acids | HP:0010995 | ||
phenodb:2790 | KEY LABORATORY ABNORMALITIES: In urine > Glycosaminoglycans (aka GAGs or Mucopolysaccharides or MPS) | HP:0008155 | T2649 | |
phenodb:2791 | KEY LABORATORY ABNORMALITIES: In urine > Glycosaminoglycans (aka GAGs or Mucopolysaccharides or MPS) > Specify | |||
phenodb:2792 | KEY LABORATORY ABNORMALITIES: In urine > Oligosaccharides | HP:0010471 | T2650 | |
phenodb:2793 | KEY LABORATORY ABNORMALITIES: In urine > Oligosaccharides > Specify | |||
phenodb:2794 | KEY LABORATORY ABNORMALITIES: In urine > Organic acids | HP:0001992 | T2638 | |
phenodb:2795 | KEY LABORATORY ABNORMALITIES: In urine > Organic acids > 3-methylglutaconic acid | HP:0003535 | ||
phenodb:2796 | KEY LABORATORY ABNORMALITIES: In urine > Organic acids > Ethylmalonic acid | HP:0003219 | ||
phenodb:2797 | KEY LABORATORY ABNORMALITIES: In urine > Organic acids > Methylmalonic acid | HP:0002912 | ||
phenodb:2798 | KEY LABORATORY ABNORMALITIES: In urine > Organic acids > Other, specify | |||
phenodb:2799 | KEY LABORATORY ABNORMALITIES: In urine > Orotic acid | HP:0003218 | ||
phenodb:3595 | KEY LABORATORY ABNORMALITIES: In urine > Porphyrins | HP:0010473 | T2663 | |
phenodb:2800 | KEY LABORATORY ABNORMALITIES: In urine > Phosphoethanolamine | HP:0003239 | ||
phenodb:2801 | KEY LABORATORY ABNORMALITIES: In urine > Other, specify | |||
phenodb:2802 | KEY LABORATORY ABNORMALITIES: In urine > Other, specify | |||
phenodb:2803 | KEY LABORATORY ABNORMALITIES: In urine > Other, specify | |||
phenodb:2804 | KEY LABORATORY ABNORMALITIES: In CSF | |||
phenodb:2805 | KEY LABORATORY ABNORMALITIES: In CSF > 5-hydroxyindoleacetic acid (5HIAA), decreased | |||
phenodb:2806 | KEY LABORATORY ABNORMALITIES: In CSF > Biopterin | |||
phenodb:2807 | KEY LABORATORY ABNORMALITIES: In CSF > Glucose, decreased | HP:0011972 | ||
phenodb:2808 | KEY LABORATORY ABNORMALITIES: In CSF > Glycine, increased | |||
phenodb:2809 | KEY LABORATORY ABNORMALITIES: In CSF > Homovanillic acid (HVA), decreased | HP:0003785 | ||
phenodb:2810 | KEY LABORATORY ABNORMALITIES: In CSF > Hypocretin, decreased | |||
phenodb:2811 | KEY LABORATORY ABNORMALITIES: In CSF > Lactate, increased | HP:0002490 | ||
phenodb:2812 | KEY LABORATORY ABNORMALITIES: In CSF > Neopterin | |||
phenodb:2813 | KEY LABORATORY ABNORMALITIES: In CSF > Protein, increased | HP:0002922 | ||
phenodb:2814 | KEY LABORATORY ABNORMALITIES: In CSF > Serine, decreased | |||
phenodb:2815 | KEY LABORATORY ABNORMALITIES: In CSF > Serotonin | |||
phenodb:2816 | KEY LABORATORY ABNORMALITIES: In CSF > Serotonin > Increased | |||
phenodb:2817 | KEY LABORATORY ABNORMALITIES: In CSF > Serotonin > Decreased | |||
phenodb:2818 | KEY LABORATORY ABNORMALITIES: In CSF > Pleocytosis | HP:0012229 | ||
phenodb:2819 | KEY LABORATORY ABNORMALITIES: In CSF > Other, specify | |||
phenodb:2820 | KEY LABORATORY ABNORMALITIES: Others | |||
phenodb:2821 | KEY LABORATORY ABNORMALITIES: Others > Chromosome breakage, increased (aka DEB testing) | HP:0003220 | T2820 | |
phenodb:2822 | KEY LABORATORY ABNORMALITIES: Others > Sweat chloride, elevated | HP:0012236 | ||
phenodb:2823 | KEY LABORATORY ABNORMALITIES: Others > Cellular sensitivity to UV light, increased | HP:0003224 | ||
phenodb:2824 | KEY LABORATORY ABNORMALITIES: Others > Other, specify | |||
phenodb:2825 | KEY LABORATORY ABNORMALITIES: Others > Other, specify | |||
phenodb:2826 | KEY LABORATORY ABNORMALITIES: Others > Other, specify |