Disease #00096

Official abbreviation	COXPD2
Name	Combined oxidative phosphorylation deficiency 2, 610498 (3)
OMIM ID	610498
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	MRPS16
Associated tissues	-
Disease features	-
Remarks	-