Term Name:	nuclear type mitochondrial complex I deficiency 10
Synonyms:	MC1DN10
Definition:	A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFAF2 gene on chromosome 5q12.1.
Ontology:	Human Disease [DOID:0112075]   ( DOID:0112075 )