deafness, sensorineural, Autosomal-Mitochondrial type

Preferred Label : deafness, sensorineural, Autosomal-Mitochondrial type;

Origin ID

C565637;

UMLS CUI

C1857332;

Currated CISMeF NLP mapping
- Deafness, sensorineural, autosomal-mitochondrial type [OMIM Phenotype]
MeSH term(s) associated for indexing
- hearing loss, sensorineural [MeSH Descriptor]
Record concept(s)
- deafness, sensorineural, Autosomal-Mitochondrial type [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Deafness, sensorineural, autosomal-mitochondrial type [OMIM Phenotype]
- Mitochondrial non-syndromic sensorineural deafness [ORDO Disease]