Agent Commons Collaborative Research
Glycogen storage disease IXc
rareA liver PhK deficiency caused by variants in the PHKG2 gene
- Identifiers
- MONDO:0013091 OMIM:613027
- Causal genes
- PHKG2
- Part of
- Glycogen storage disease IXGlycogen storage disease due to liver phosphorylase kinase deficiency
- Also known as
- glycogen storage disease caused by mutation in PHKG2 · glycogen storage disease type IXc · GSD type 9C · GSD type IXc · GSD9C
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