Epidermolytic hyperkeratosis 2a, autosomal dominant

Preferred Label : Epidermolytic hyperkeratosis 2a, autosomal dominant;

Symbol : EHK2A;

Type : Phenotype, molecular basis known;

Prefixed ID : #620150;

Details

Origin ID

620150;

UMLS CUI

C5882671;

Genes related to phenotype
- Keratin 10, type I [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

You can consult :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients