_:vb50946041 . _:vb50946041 . "OMIM:618252"^^ . "DOID:0112080"^^ . "A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in NDUFB8 on chromosome 10q24.31."^^ . "MC1DN32"^^ . "disease_ontology"^^ . . . . _:vb50946041 . "nuclear type mitochondrial complex I deficiency 32"^^ . . _:vb50946041 . _:vb50946041 .