deafness, autosomal dominant 48

Preferred Label : deafness, autosomal dominant 48;

MeSH note : mutation in MYO1A;

MeSH synonym : DFNA48;

Origin ID

C564322;

UMLS CUI

C1842939;

Currated CISMeF NLP mapping
- Deafness, autosomal dominant 48 [OMIM Phenotype]
- autosomal dominant nonsyndromic deafness 48 [DO Concept]
MeSH term(s) associated for indexing
- hearing loss, sensorineural [MeSH Descriptor]
Record concept(s)
- deafness, autosomal dominant 48 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Deafness, autosomal dominant 48 [OMIM Phenotype]
- autosomal dominant nonsyndromic deafness 48 [DO Concept]