Alopecia

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 6
OrphanetNr: 79364
OMIM Id:
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: Genetic hair anomaly
 -Rare genetic disease
Hair anomaly
 -Rare skin disease

Symptom Information: Sort by abundance 

1
 (HPO:0100840) Aplasia/Hypoplasia of the eyebrow Very frequent [Orphanet] 117 / 7739
2
 (HPO:0000606) Abnormality of the periorbital region Very frequent [Orphanet] 96 / 7739
3
 (HPO:0001006) Hypotrichosis Very frequent [Orphanet] 219 / 7739
4
 (HPO:0001596) Alopecia Very frequent [Orphanet] 162 / 7739
5
 (HPO:0002225) Sparse pubic hair Very frequent [Orphanet] 76 / 7739
6
 (HPO:0030350) Erythematous papule Very frequent [Orphanet] 123 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: