albinism-deafness syndrome

Preferred Label : albinism-deafness syndrome;

Obsolete resource : true;

Approved symbol HGNC : ADFN;

Chromosome HGNC : Xq26.3-q27.1;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:247;

UMLS CUI

C1412233;

Automatic exact mappings (from CISMeF team)
- Albinism-deafness syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

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