Disease #00099

Official abbreviation	COXPD5
Name	Combined oxidative phosphorylation deficiency 5, 611719 (3)
OMIM ID	611719
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	MRPS22
Associated tissues	-
Disease features	-
Remarks	-