Disease #00022

Official abbreviation	MC3DN6
Name	Mitochondrial complex III deficiency, nuclear type 6, 615453 (3)
OMIM ID	615453
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	CYC1
Associated tissues	-
Disease features	-
Remarks	-