Term Name:	nuclear type mitochondrial complex I deficiency 6
Synonyms:	MC1DN6
Definition:	A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFS2 gene on chromosome 1q23.
Ontology:	Human Disease [DOID:0112066]   ( DOID:0112066 )