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Echinobase
Summary Literature (0)
MIM:611719 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5; COXPD5

Echinobase Genes: mrps22

Human Disease Resource: OMIM


Disease Ontology (DO):
DOID:0060286 - combined oxidative phosphorylation deficiency
DOID:0111473 - combined oxidative phosphorylation deficiency 5