deafness, autosomal dominant 2A

Preferred Label : deafness, autosomal dominant 2A;

MeSH synonym : DFNA2A;

Origin ID

C567441;

UMLS CUI

C2677637;

Currated CISMeF NLP mapping
- Deafness, autosomal dominant 2a [OMIM Phenotype]
- autosomal dominant nonsyndromic deafness 2A [DO Concept]
MeSH term(s) associated for indexing
- hearing loss, sensorineural [MeSH Descriptor]
Record concept(s)
- deafness, autosomal dominant 2A [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Deafness, autosomal dominant 2a [OMIM Phenotype]
- autosomal dominant nonsyndromic deafness 2A [DO Concept]