"DOID:0112085"^^ . "OMIM:618241"^^ . "A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in FOXRED1 on chromosome 11q24.2."^^ . . "MC1DN19"^^ . "nuclear type mitochondrial complex I deficiency 19"^^ . _:vb50946051 . _:vb50946051 . "disease_ontology"^^ . . . _:vb50946051 . _:vb50946051 . _:vb50946051 . .