Alopecia totalis

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 7
OrphanetNr: 700
OMIM Id: 104000
300042
610753
ICD-10: L63.0
UMLs: C0263504
MeSH:
MedDRA: 10001766
Snomed: 19754005

Prevalence, inheritance and age of onset:

Prevalence: 10.5 of 100 000 [Orphanet]
Inheritance:
Age of onset: All ages
[Orphanet]

Disease classification (adopted from Orphanet):

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

Symptom Information: Sort by abundance 

1
 (HPO:0001596) Alopecia Very frequent [Orphanet] 162 / 7739
2
 (HPO:0001803) Nail pits 17 / 7739
3
 (HPO:0001006) Hypotrichosis Very frequent [Orphanet] 219 / 7739
4
 (HPO:0007418) Alopecia totalis 6 / 7739
5
 (HPO:0002229) Alopecia areata 5 / 7739
6
 (HPO:0002960) Autoimmunity 78 / 7739
7
 (HPO:0001426) Multifactorial inheritance 37 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: