glycogen storage disease IXa

Summary
Synonym
  • GSD type 9A
  • GSD type IXa
  • GSD9A
  • glycogen storage disease type 9A
  • glycogen storage disease type IXa
  • glycogenosis type 9A
  • glycogenosis type IXa
Definition
A glycogen storage disease IX characterized by hepatomegaly, growth retardation, elevation of glutamate-pyruvate transaminase and glutamate-oxaloacetate transaminase, hypercholesterolemia, hypertriglyceridemia, and fasting hyperketosis, but symptoms gradually disappear with age, that has_material_basis_in X-linked inheritance of mutation in the PHKA2 gene on chromosome Xp22.
Super Class
X-linked recessive disease glycogen storage disease IX
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
5256 PHKA2 phosphorylase kinase regulatory subunit alpha 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
110094 Phka2 phosphorylase kinase alpha 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
31839 CG7766 uncharacterized protein
Displaying 1 entry
Gene ID Gene Symbol Description Source
176149 C14B9.8 Phosphorylase b kinase regulatory subunit;putative phosphorylase b kinase regulatory subunit alpha

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024