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Nonsyndromic sensorineural hearing loss MeSH Supplementary Concept Data 2022


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 Number
0
Heading Mapped to
*Hearing Loss, Sensorineural
Frequency
120
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 Preferred
Deafness, nonsyndromic sensorineural, mitochondrial Related
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