Term Name:	nuclear type mitochondrial complex I deficiency 26
Synonyms:	MC1DN26
Definition:	A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFA9 gene on chromosome 12p13.32.
Ontology:	Human Disease [DOID:0112086]   ( DOID:0112086 )