Disease #00518

Official abbreviation	616539
Name	Combined oxidative phosphorylation deficiency 26, 616539 (3)
OMIM ID	616539
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	TRMT5
Associated tissues	-
Disease features	-
Remarks	-