deafness, autosomal dominant 2B

Preferred Label : deafness, autosomal dominant 2B;

MeSH synonym : DFNA2B;

Origin ID

C567214;

UMLS CUI

C2675236;

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