Nonsyndromic sensorineural hearing loss [Supplementary Concept]
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 introduced: August 25, 2010
MeSH Unique ID: C537845
Heading Mapped to:
Entry Terms:
- Autosomal dominant nonsyndromic hereditary hearing impairment
- Nonsyndromic hereditary hearing impairment
- Deafness, nonsyndromic sensorineural, mitochondrial