MeSH Browser

MeSH Supplementary: Nonsyndromic Deafness
Unique ID: C580334
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C580334
Entry Term(s): Isolated Deafness; Nonsyndromic Hearing Impairment; Nonsyndromic Hearing Loss; Undifferentiated Deafness
Registry Numbers: 0
Heading Mapped to: *Deafness
Frequency: 279
Note: Hearing loss that is not associated with other signs and symptoms. Most cases are due to damage to structures of the INNER EAR. More than half of congenital cases are due to genetic factors; mutations in multiple genes have been identified, including POU3F4 (OMIM: 304400), MTRNR1 (OMIM: 561000), and MT-TS1 (OMIM: 590080).
Date of Entry: 2013/10/24
Revision Date: 2016/07/07

Concept UI: M0583780
Registry Numbers: 0
Terms: Nonsyndromic Deafness Preferred Term
Term UI T842148
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Isolated Deafness
Term UI T842149
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Nonsyndromic Hearing Impairment
Term UI T842150
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Nonsyndromic Hearing Loss
Term UI T842151
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Undifferentiated Deafness
Term UI T842152
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014)

Nonsyndromic Deafness MeSH Supplementary Concept Data 2025