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 21 - 30 of 30 in total
Gene ID Gene Symbol Description Source
5236 PGM1 phosphoglucomutase 1
5261 PHKG2 phosphorylase kinase catalytic subunit gamma 2
5837 PYGM glycogen phosphorylase, muscle associated
6476 SI sucrase-isomaltase
6514 SLC2A2 solute carrier family 2 member 2
7957 EPM2A EPM2A glucan phosphatase, laforin
8908 GYG2 glycogenin 2
8972 MGAM maltase-glucoamylase
57818 G6PC2 glucose-6-phosphatase catalytic subunit 2
92579 G6PC3 glucose-6-phosphatase catalytic subunit 3
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