All diseases

OMIM ID
261650
OMIM term:
PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, MITOCHONDRIAL
Alternative terms:
PCK2 DEFICIENCY
PEPCK2 DEFICIENCY
(∗) Location:
14q11.2  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/2qnm4svs