MeSH Browser

MeSH Supplementary: Auditory neuropathy
Unique ID: C538268
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538268
Entry Term(s): Auditory dys-synchrony; Familial auditory neuropathy; Progressive auditory neuropathy
Heading Mapped to: *Hearing Loss, Central
Frequency: 324
Note: A hearing disorder in which sound enters the INNER EAR normally but the transmission of signals from the inner ear to the brain is impaired. Germline mutations in the OTOF gene have been identified for Auditory Neuropathy, Autosomal Recessive, 1 (OMIM: 601071)
Date of Entry: 2010/08/25
Revision Date: 2015/08/17

Concept UI: M0532729
Terms: Auditory neuropathy Preferred Term
Term UI T745262
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Auditory dys-synchrony
Term UI T745263
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Familial auditory neuropathy
Term UI T753725
Date07/01/2009
LexicalTag NON
ThesaurusID ORD (2010); Progressive auditory neuropathy
Term UI T753726
Date07/01/2009
LexicalTag NON
ThesaurusID ORD (2010)

Auditory neuropathy MeSH Supplementary Concept Data 2024