Congenital, generalized hypertrichosis
Symptom Information:
Symptom ID: | HPO:0004540 | ||||
Synonyms: |
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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) Hypertrichosis(HPO:0000998) Congenital, generalized hypertrichosis(HPO:0004540) MedDRA: |
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Database Frequency: | 11 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Acquired hypertrichosis lanuginosa | (Orphanet:2221) |
Congenital generalized hypertrichosis, Ambras type | (Orphanet:1023) |
Gingival fibromatosis-hypertrichosis syndrome | (Orphanet:2026) |
HYPERTRICHOSIS LANUGINOSA CONGENITA | (OMIM:145700) |
Hypertrichosis lanuginosa congenita | (Orphanet:2222) |
Hypertrichotic osteochondrodysplasia, Cantu type | (Orphanet:1517) |
Hypotrichosis simplex | (Orphanet:55654) |
Lethal restrictive dermopathy | (Orphanet:1662) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Steatocystoma multiplex - natal teeth | (Orphanet:3184) |
X-linked congenital generalized hypertrichosis | (Orphanet:79495) |