Disease #00018

Official abbreviation	MC3DN2
Name	Mitochondrial complex III deficiency, nuclear type 2, 615157 (3)
OMIM ID	615157
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	TTC19
Associated tissues	-
Disease features	-
Remarks	-