Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:220111 - MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 5; MC4DN5

Xenbase Genes: lrpprc

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009069 - congenital lactic acidosis, Saguenay-Lac-Saint-Jean type

Disease Ontology (DO):
DOID:0111180 - French Canadian Leigh disease
DOID:3652 - Leigh disease