Disease #00521

Official abbreviation	616974
Name	Combined oxidative phosphorylation deficiency 30, 616974 (3)
OMIM ID	616974
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	TRMT10C
Associated tissues	-
Disease features	-
Remarks	-