OBO ID: DOID:0111751 |
Term Name: | mitochondrial nonsyndromic sensorineural deafness | Search Ontology: | |
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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) | ||
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Ontology: | Human Disease (DOID:0111751) |
OTHER mitochondrial nonsyndromic sensorineural deafness PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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