Disease #00515

Official abbreviation	615917
Name	Combined oxidative phosphorylation deficiency 20, 615917 (3)
OMIM ID	615917
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	VARS2
Associated tissues	-
Disease features	-
Remarks	-