Term Name:	nuclear type mitochondrial complex I deficiency 3
Synonyms:	MC1DN3
Definition:	A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFS7 gene on chromosome 19p13.3.
Ontology:	Human Disease [DOID:0112093]   ( DOID:0112093 )