Term Name:	nuclear type mitochondrial complex I deficiency 13
Synonyms:	MC1DN13
Definition:	A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFA2 gene on chromosome 5q31.3.
Ontology:	Human Disease [DOID:0112076]   ( DOID:0112076 )