Term Name:	nuclear type mitochondrial complex I deficiency 9
Synonyms:	MC1DN9
Definition:	A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFS6 gene on chromosome 5p15.33.
Ontology:	Human Disease [DOID:0112073]   ( DOID:0112073 )