Disease #00514

Official abbreviation	615578
Name	Combined oxidative phosphorylation deficiency 18, 615578 (3)
OMIM ID	615578
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	SFXN4
Associated tissues	-
Disease features	-
Remarks	-