deafness, autosomal dominant 6

Preferred Label : deafness, autosomal dominant 6;

MeSH note : mutation in WFS1;

MeSH synonym : DFNA6; DFNA14; DFNA38; deafness, autosomal dominant 14; deafness, autosomal dominant 38;

Details

Origin ID

C563421;

UMLS CUI

C1833021;

Currated CISMeF NLP mapping
- Deafness, autosomal dominant 6 [OMIM Phenotype]
- autosomal dominant nonsyndromic deafness 6 [DO Concept]
MeSH term(s) associated for indexing
- hearing loss, sensorineural [MeSH Descriptor]
Record concept(s)
- deafness, autosomal dominant 6 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Deafness, autosomal dominant 6 [OMIM Phenotype]
- autosomal dominant nonsyndromic deafness 6 [DO Concept]

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