Disease #00019

Official abbreviation	MC3DN3
Name	Mitochondrial complex III deficiency, nuclear type 3, 615158 (3)
OMIM ID	615158
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 2 genes	, UQCRB
Associated tissues	-
Disease features	-
Remarks	-