glycogen storage disease IXc

Summary
Synonym
  • GSD type 9C
  • GSD type IXc
  • GSD9C
  • glycogen storage disease type 9C
  • glycogen storage disease type IXc
  • glycogenosis type 9C
  • glycogenosis type IXc
Definition
A glycogen storage disease IX characterized by autosomal recessive inheritance of hepatomegaly, hypotonia, growth retardation, and liver dysfunction with onset in childhood and improvement of symptoms with age that has_material_basis_in homozygous and compound heterozygous mutation in the PHKG2 gene on chromosome 16p11.
Super Class
autosomal 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
68961 Phkg2 phosphorylase kinase, gamma 2 (testis)
Displaying 1 entry
Gene ID Gene Symbol Description Source
140671 Phkg2 phosphorylase kinase catalytic subunit gamma 2

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Last updated: August 19, 2024