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:615595 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 19; COXPD19

Xenbase Genes: lyrm4

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014269 - combined oxidative phosphorylation deficiency 19
MONDO:0018337 - obsolete severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency

Disease Ontology (DO):
DOID:0060286 - combined oxidative phosphorylation deficiency
DOID:0111476 - combined oxidative phosphorylation deficiency 19