Disease #00520

Official abbreviation	616794
Name	Combined oxidative phosphorylation deficiency 28, 616794 (3)
OMIM ID	616794
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	SLC25A26
Associated tissues	-
Disease features	-
Remarks	-