Term Name:	nuclear type mitochondrial complex I deficiency 7
Synonyms:	MC1DN7
Definition:	A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFV2 gene on chromosome 18p11.22.
Ontology:	Human Disease [DOID:0112092]   ( DOID:0112092 )