Disease #00093

Official abbreviation	COXPD10
Name	Combined oxidative phosphorylation deficiency 10, 614702 (3)
OMIM ID	614702
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	MTO1
Associated tissues	-
Disease features	-
Remarks	-