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Summary Literature (0)
MIM:615595 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 19; COXPD19

Xenbase Genes: lyrm4

Human Disease Resource: MIM

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