MeSH Browser

MeSH Supplementary: Nonsyndromic sensorineural hearing loss
Unique ID: C537845
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537845
Entry Term(s): Autosomal dominant nonsyndromic hereditary hearing impairment; Deafness, nonsyndromic sensorineural, mitochondrial; Nonsyndromic hereditary hearing impairment
Registry Numbers: 0
Heading Mapped to: *Hearing Loss, Sensorineural
Frequency: 123
Note: Partial or total loss of hearing that is not associated with other signs and symptoms. Some hereditary cases may be caused by mutations in MITOCHONDRIAL GENES. OMIM: 500008
Date of Entry: 2010/08/25
Revision Date: 2016/07/19

Nonsyndromic sensorineural hearing loss MeSH Supplementary Concept Data 2025