Disease #00513

Official abbreviation	615440
Name	Combined oxidative phosphorylation deficiency 17, 615440 (3)
OMIM ID	615440
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	ELAC2
Associated tissues	-
Disease features	-
Remarks	-