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Summary Literature (0)
MIM:261650 - PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, MITOCHONDRIAL; PCKDM

Xenbase Genes: pck2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009864 - phosphoenolpyruvate carboxykinase deficiency, mitochondrial
MONDO:0017320 - phosphoenolpyruvate carboxykinase deficiency