"DOID:0112139"^^ . _:vb50946165 . _:vb50946165 . . _:vb50946165 . "OMIM:619003"^^ . . "disease_ontology"^^ . _:vb50946165 . "nuclear type mitochondrial complex I deficiency 35"^^ . "MC1DN35"^^ . . . "A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in NDUFB10 on chromosome 16p13.3."^^ . _:vb50946165 .