_:vb50938690 . . "DOID:0060351"^^ . "mitochondrial complex III deficiency nuclear type 2"^^ . "A mitochondrial metabolism disease characterized by motor disability, with ataxia, apraxia, dystonia, and dysarthria, associated with necrotic lesions throughout the brain and has_material_basis_in mutation in the TTC19 gene on chromosome 17. It has an autosomal recessive inheritance pattern."^^ . "OMIM:615157"^^ . . _:vb50938690 . _:vb50938690 . "2015-07-14T16:24:56Z"^^ . "disease_ontology"^^ . . "MC3DN2"@en . "elvira"^^ . . _:vb50938690 . _:vb50938690 .