Disease #00501

Official abbreviation	615918
Name	?Combined oxidative phosphorylation deficiency 21, 615918 (3)
OMIM ID	615918
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	TARS2
Associated tissues	-
Disease features	-
Remarks	-