deafness, autosomal dominant 40

Preferred Label : deafness, autosomal dominant 40;

Obsolete resource : true;

Approved symbol HGNC : DFNA40;

Chromosome HGNC : 16p12;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:14070;

UMLS CUI

C1422388;

See also inter- (CISMeF)
- Deafness, autosomal dominant 40 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

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