Congenital, generalized hypertrichosis

Symptom Information:

Symptom ID: HPO:0004540
Synonyms:
Congenital generalized hypertrichosis [HPO:0004540]
Hypertrichosis universalis [HPO:0004540]
Congenital, generalized hypertrichosis [OMIM:Congenital, generalized hypertrichosis]
Hypertrichosis universalis [OMIM:Hypertrichosis universalis]
Quality:
Cross references:
OMIM: "Congenital, generalized hypertrichosis" [OMIM:Congenital, generalized hypertrichosis]
OMIM: "Hypertrichosis universalis" [OMIM:Hypertrichosis universalis]
Is a (Direct Parents):
HPO         Hypertrichosis
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:
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)