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Summary Literature (0)
DOID:0111751 - mitochondrial nonsyndromic sensorineural deafness


Disease Ontology Definition:A sensorineural hearing loss that has_material_basis_in mutation in one of several different mitochondrial genes including; MTRNR1, MTTS1, MTCO1, MTTH, MTND1, and MTTI.

Synonyms:

In OMIM:
OMIM:500008 - DEAFNESS, NONSYNDROMIC SENSORINEURAL, MITOCHONDRIAL


Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : cox1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): sensorineural hearing loss (is_a)