auditory neuropathy, nonsyndromic recessive

Preferred Label : auditory neuropathy, nonsyndromic recessive;

MeSH note : mutation in otoferlin;

Origin ID

C563398;

UMLS CUI

C1832830;

Automatic exact mappings (from CISMeF team)
- Deafness, autosomal recessive 9 [OMIM Phenotype]
MeSH term(s) associated for indexing
- hearing loss, sensorineural [MeSH Descriptor]
Record concept(s)
- auditory neuropathy, nonsyndromic recessive [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]