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 (1)
MIM:617713 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 33; COXPD33

Xenbase Genes: c1qbp

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0054677 - combined oxidative phosphorylation deficiency 33

Disease Ontology (DO):
DOID:0111495 - combined oxidative phosphorylation deficiency 33