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:615440 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17; COXPD17

Xenbase Genes: elac2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014190 - combined oxidative phosphorylation defect type 17

Disease Ontology (DO):
DOID:0111496 - combined oxidative phosphorylation deficiency 17