Disease #00519

Official abbreviation	616672
Name	Combined oxidative phosphorylation deficiency 27, 616672 (3)
OMIM ID	616672
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	CARS2
Associated tissues	-
Disease features	-
Remarks	-