ALOPECIA, CONGENITAL

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 5
OrphanetNr:
OMIM Id: 300042
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
(HPO:0001596) Alopecia 162 / 7739
2
(HPO:0001006) Hypotrichosis 219 / 7739
3
(OMIM) Normal eyebrows and eyelashes 2 / 7739
4
(HPO:0001417) X-linked inheritance 173 / 7739
5
(OMIM) Congenital scalp alopecia 1 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information:

Clinical Description OMIM Anzai et al. (1996) described a Japanese family in which 3 boys in 3 separate sibships related as first cousins through the mother in each case had congenital alopecia or marked hypotrichosis. None of the 3 mothers had ...