deafness, autosomal dominant 47

Preferred Label : deafness, autosomal dominant 47;

MeSH synonym : DFNA47;

Origin ID

C563885;

UMLS CUI

C1837609;

Currated CISMeF NLP mapping
- Deafness, autosomal dominant 47 [OMIM Phenotype]
- autosomal dominant nonsyndromic deafness 47 [DO Concept]
MeSH term(s) associated for indexing
- hearing loss, sensorineural [MeSH Descriptor]
Record concept(s)
- deafness, autosomal dominant 47 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Deafness, autosomal dominant 47 [OMIM Phenotype]
- autosomal dominant nonsyndromic deafness 47 [DO Concept]