_:vb50946069 . _:vb50946069 . _:vb50946069 . "DOID:0112094"^^ . "disease_ontology"^^ . . _:vb50946069 . "A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in NDUFA11 on chromosome 19p13.3."^^ . "OMIM:618236"^^ . "MC1DN14"^^ . . . . _:vb50946069 . "nuclear type mitochondrial complex I deficiency 14"^^ .