Disease #00511

Official abbreviation	614924
Name	Combined oxidative phosphorylation deficiency 12, 614924 (3)
OMIM ID	614924
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	EARS2
Associated tissues	-
Disease features	-
Remarks	-