Hypotrichosis simplex of the scalp

General Information (adopted from Orphanet):

Synonyms, Signs: Hereditary hypotrichosis simplex of the scalp
Number of Symptoms 2
OrphanetNr: 90368
OMIM Id: 146520
613981
ICD-10: L65.8
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal dominant
[Orphanet]
Age of onset: Childhood
[Orphanet]

Disease classification (adopted from Orphanet):

Parent Diseases: Alopecia
 -Rare genetic disease
 -Rare skin disease

Symptom Information: Sort by abundance 

1
(HPO:0004782) Hypotrichosis of the scalp 7 / 7739
2
(HPO:0000006) Autosomal dominant inheritance 2518 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: