deafness, autosomal dominant 20

Preferred Label : deafness, autosomal dominant 20;

MeSH note : mutation in ACTG1;

MeSH synonym : DFNA26; DFNA20;

Origin ID

C565754;

UMLS CUI

C1858172;

Currated CISMeF NLP mapping
- Deafness, autosomal dominant 20 [OMIM Phenotype]
- autosomal dominant nonsyndromic deafness 20 [DO Concept]
MeSH term(s) associated for indexing
- hearing loss, sensorineural [MeSH Descriptor]
Record concept(s)
- deafness, autosomal dominant 20 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Deafness, autosomal dominant 20 [OMIM Phenotype]
- autosomal dominant nonsyndromic deafness 20 [DO Concept]