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DOID:0050757 - deafness-dystonia-optic neuronopathy syndrome
Disease Ontology Definition:A mitochondrial metabolism disease that is characterized by hearing loss that begins early in life, problems with movement, impaired vision, and behavior problems, and has_material_basis_in mutations in the TIMM8A gene resulting in abnormal protein transport within the mitochondria.
Synonyms: Deafness Dystonia Optic Atrophy Syndrome, Deafness Dystonia Optic Neuronopathy Syndrome, Deafness Dystonia Optic Neuronopathy Syndrome (DDON), Dystonia Deafness Syndrome, Jensen syndrome, Mohr-Tranebjaerg Syndrome, Mohr-Tranebjaerg syndrome, deafness dystonia syndrome,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0010578 - deafness dystonia syndrome |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee