deafness, autosomal dominant 36

Preferred Label : deafness, autosomal dominant 36;

MeSH synonym : DFNA36;

Origin ID

C564675;

UMLS CUI

C1847626;

Currated CISMeF NLP mapping
- Deafness, Autosomal Dominant 36 [NCIt concept]
- Deafness, autosomal dominant 36 [OMIM Phenotype]
- autosomal dominant nonsyndromic deafness 36 [DO Concept]
MeSH term(s) associated for indexing
- hearing loss, sensorineural [MeSH Descriptor]
Record concept(s)
- deafness, autosomal dominant 36 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Deafness, Autosomal Dominant 36 [NCIt concept]
- Deafness, autosomal dominant 36 [OMIM Phenotype]
- autosomal dominant nonsyndromic deafness 36 [DO Concept]