Term Name:	nuclear type mitochondrial complex I deficiency 33
Synonyms:	MC1DN33
Definition:	A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFA6 gene on chromosome 22q13.2.
Ontology:	Human Disease [DOID:0112097]   ( DOID:0112097 )