Deafness, autosomal dominant 87

Preferred Label : Deafness, autosomal dominant 87;

Symbol : DFNA87;

Type : Phenotype, molecular basis known;

Prefixed ID : #620281;

Details

Origin ID

620281;

UMLS CUI

C5830342;

Genes related to phenotype
- Phosphatidylinositol 4-kinase, beta [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