Abnormal hair quantity
Symptom Information:
| Symptom ID: | HPO:0011362 | ||
| Synonyms: |
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| Quality: | |||
| Cross references: |
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| Is a (Direct Parents): |
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| Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the integument(HPO:0001574) Abnormality of skin adnexa(HPO:0011138) Abnormality of the hair(HPO:0001595) Abnormal hair quantity(HPO:0011362) MedDRA: |
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| Database Frequency: | 92 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| 17q21.31 microduplication syndrome | (Orphanet:217340) |
| 19p13.12 microdeletion syndrome | (Orphanet:254346) |
| 1p36 deletion syndrome | (Orphanet:1606) |
| 2q23.1 microdeletion syndrome | (Orphanet:228402) |
| 4q21 microdeletion syndrome | (Orphanet:238750) |
| ACTH-dependent Cushing syndrome | (Orphanet:99892) |
| ACTH-independent Cushing syndrome | (Orphanet:99893) |
| ACTH-independent macronodular adrenal hyperplasia | (Orphanet:189427) |
| AREDYLD syndrome | (Orphanet:1133) |
| Acanthosis nigricans | (Orphanet:924) |
| Acquired hypertrichosis lanuginosa | (Orphanet:2221) |
| Acromegaly | (Orphanet:963) |
| Acroosteolysis, dominant type | (Orphanet:955) |
| Argininosuccinic aciduria | (Orphanet:23) |
| Autosomal dominant popliteal pterygium syndrome | (Orphanet:1300) |
| Barber-Say syndrome | (Orphanet:1231) |
| Bohring-Opitz syndrome | (Orphanet:97297) |
| Brachymorphism - onychodysplasia - dysphalangism | (Orphanet:1292) |
| Castleman disease | (Orphanet:160) |
| Cataract - deafness - hypogonadism | (Orphanet:1383) |
| Cataract - hypertrichosis - intellectual deficit | (Orphanet:1375) |
| Cervical hypertrichosis - peripheral neuropathy | (Orphanet:2218) |
| Classical phenylketonuria | (Orphanet:79254) |
| Coffin-Siris syndrome | (Orphanet:1465) |
| Congenital erythropoietic porphyria | (Orphanet:79277) |
| Cornelia de Lange syndrome | (Orphanet:199) |
| Craniofaciofrontodigital syndrome | (Orphanet:363705) |
| Curry-Jones syndrome | (Orphanet:1553) |
| Cushing syndrome due to ectopic ACTH secretion | (Orphanet:99889) |
| Cyprus facial-neuromusculoskeletal syndrome | (Orphanet:2674) |
| Dahlberg-Borer-Newcomer syndrome | (Orphanet:1563) |
| Diastematomyelia | (Orphanet:1671) |
| Dwarfism - intellectual deficit - eye abnormality | (Orphanet:2650) |
| Ectodermal dysplasia, Berlin type | (Orphanet:1816) |
| Edinburgh malformation syndrome | (Orphanet:1895) |
| Epilepsy - microcephaly - skeletal dysplasia | (Orphanet:1948) |
| Erythrokeratodermia variabilis | (Orphanet:317) |
| Fetal alcohol syndrome | (Orphanet:1915) |
| Fetal minoxidil syndrome | (Orphanet:1918) |
| Floating-Harbor syndrome | (Orphanet:2044) |
| GM1 gangliosidosis | (Orphanet:354) |
| Gingival fibromatosis-hypertrichosis syndrome | (Orphanet:2026) |
| Gorlin-Chaudhry-Moss syndrome | (Orphanet:2095) |
| Grix-Blankenship-Peterson syndrome | (Orphanet:2099) |
| Hawkinsinuria | (Orphanet:2118) |
| Hirsutism - skeletal dysplasia - intellectual deficit | (Orphanet:2156) |
| Hurler syndrome | (Orphanet:93473) |
| Hurler-Scheie syndrome | (Orphanet:93476) |
| Hypertrichosis | (Orphanet:79365) |
| Hypertrichosis cubiti - short stature | (Orphanet:2220) |
| Hypertrichosis lanuginosa congenita | (Orphanet:2222) |
| Hypertrichotic osteochondrodysplasia, Cantu type | (Orphanet:1517) |
| Intellectual deficit, X-linked - hypogammaglobulinemia - progressive neurological deterioration | (Orphanet:85317) |
| Ito hypomelanosis | (Orphanet:435) |
| Large congenital melanocytic nevus | (Orphanet:626) |
| Lowry-MacLean syndrome | (Orphanet:2409) |
| Mal de Meleda | (Orphanet:87503) |
| Marfanoid habitus - intellectual deficit, autosomal recessive | (Orphanet:2463) |
| Marshall-Smith syndrome | (Orphanet:561) |
| Menkes disease | (Orphanet:565) |
| Micrencephaly - corpus callosum agenesis - abnormal genitalia | (Orphanet:2508) |
| Micro syndrome | (Orphanet:2510) |
| Microlissencephaly - micromelia | (Orphanet:50810) |
| Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria | (Orphanet:1933) |
| Mucolipidosis type 2 | (Orphanet:576) |
| Mucopolysaccharidosis type 1 | (Orphanet:579) |
| Mucopolysaccharidosis type 2 | (Orphanet:580) |
| Mucopolysaccharidosis type 3 | (Orphanet:581) |
| Multiple benign circumferential skin creases on limbs | (Orphanet:2505) |
| Neurocutaneous melanocytosis | (Orphanet:2481) |
| Okamoto syndrome | (Orphanet:2729) |
| POEMS syndrome | (Orphanet:2905) |
| Papillon-Lefèvre syndrome | (Orphanet:678) |
| Parana hard-skin syndrome | (Orphanet:2812) |
| Porphyria cutanea tarda | (Orphanet:101330) |
| Porphyria due to ALA dehydratase deficiency | (Orphanet:100924) |
| Progeroid syndrome, Petty type | (Orphanet:2963) |
| Prolidase deficiency | (Orphanet:742) |
| Proteus syndrome | (Orphanet:744) |
| Pseudoleprechaunism syndrome, Patterson type | (Orphanet:2976) |
| Ramon syndrome | (Orphanet:3019) |
| Rubinstein-Taybi syndrome | (Orphanet:783) |
| Ruvalcaba syndrome | (Orphanet:3121) |
| Schinzel-Giedion syndrome | (Orphanet:798) |
| Schwartz-Jampel syndrome | (Orphanet:800) |
| Sinus node disease and myopia | (OMIM:182190) |
| Steinert myotonic dystrophy | (Orphanet:273) |
| Torg-Winchester syndrome | (Orphanet:3460) |
| Tricho-oculo-dermo-vertebral syndrome | (Orphanet:3354) |
| Trisomy 17p | (Orphanet:261290) |
| Werner syndrome | (Orphanet:902) |
| Zimmermann-Laband syndrome | (Orphanet:3473) |