Disease #00516

Official abbreviation	616198
Name	Combined oxidative phosphorylation deficiency 23, 616198 (3)
OMIM ID	616198
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	GTPBP3
Associated tissues	-
Disease features	-
Remarks	-