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
External Links
Related Genes
Displaying entries 11 - 20 of 30 in total
Gene ID Gene Symbol Description Source
2632 GBE1 1,4-alpha-glucan branching enzyme 1
2717 GLA galactosidase alpha
2992 GYG1 glycogenin 1
2998 GYS2 glycogen synthase 2
3030 HADHA hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha
3939 LDHA lactate dehydrogenase A
5211 PFKL phosphofructokinase, liver type
5213 PFKM phosphofructokinase, muscle
5224 PGAM2 phosphoglycerate mutase 2
5230 PGK1 phosphoglycerate kinase 1
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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Last updated: August 19, 2024