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mitochondrial non-syndromic sensorineural deafness

Disease Summary
Associated Targets (4)
Tbio

3

Tchem

1


GARD Rare
Uniprot Description A form of non-syndromic deafness with maternal inheritance. Affected individuals manifest progressive, postlingual, sensorineural hearing loss involving high frequencies.
Mondo Term and Equivalent IDs
MONDO:0010779:  mitochondrial non-syndromic sensorineural deafness
DOID:0111751: 
GARD:0001709: 
Orphanet:90641: