|OBO ID: DOID:0111751|
|Term Name:||mitochondrial nonsyndromic sensorineural deafness||Search 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. (5)|
|Ontology:||Human Disease (DOID:0111751)|
|is a type of:||
OTHER mitochondrial nonsyndromic sensorineural deafness PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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