Deafness, autosomal dominant 89

Preferred Label : Deafness, autosomal dominant 89;

Symbol : DFNA89;

Type : Phenotype, molecular basis known;

Prefixed ID : #620284;

Details

Origin ID

620284;

UMLS CUI

C5830357;

Genes related to phenotype
- Atonal bhlh transcription factor 1 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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