Disease #00021

Official abbreviation	MC3DN5
Name	Mitochondrial complex III deficiency, nuclear type 5, 615160 (3)
OMIM ID	615160
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	UQCRC2
Associated tissues	-
Disease features	-
Remarks	-