deafness, autosomal recessive 38

Preferred Label : deafness, autosomal recessive 38;

Obsolete resource : true;

Approved symbol HGNC : DFNB38;

Chromosome HGNC : 6q25.3-q27;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:19210;

UMLS CUI

C1426089;

See also inter- (CISMeF)
- Deafness, autosomal recessive 38 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

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