Term Name:	combined oxidative phosphorylation deficiency 29
Synonyms:	COXPD29
Definition:	A combined oxidative phosphorylation deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the TXN2 gene on chromosome 22q12.3.
Ontology:	Human Disease [DOID:0111501]   ( DOID:0111501 )