glycogen storage disease VI

Summary
Synonym
  • Glycogen storage disease 6
  • Hers' disease
  • glycogen storage disease type VI
  • hepatic glycogen phosphorylase deficiency
  • hepatophosphorylase deficiency glycogenosis
Definition
A glycogen storage disease characterized by enlargement of the liver, moderately low blood sugar, elevated levels of acetone and other ketone bodies in the blood and moderate growth retardation.
Super Class
autosomal recessive disease glycogen storage disease
External Links
Disease Ontology
DOID:2754
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying all 9 entries
Gene ID Gene Symbol Description Source
353 APRT adenine phosphoribosyltransferase
2026 ENO2 enolase 2
2538 G6PC1 glucose-6-phosphatase catalytic subunit 1
2548 GAA alpha glucosidase
2632 GBE1 1,4-alpha-glucan branching enzyme 1
3612 IMPA1 inositol monophosphatase 1
5213 PFKM phosphofructokinase, muscle
5836 PYGL glycogen phosphorylase L
5837 PYGM glycogen phosphorylase, muscle associated
Displaying 1 entry
Gene ID Gene Symbol Description Source
110095 Pygl liver glycogen phosphorylase
Displaying 1 entry
Gene ID Gene Symbol Description Source
64035 Pygl glycogen phosphorylase L
Displaying 1 entry
Gene ID Gene Symbol Description Source
33386 Glyp Glycogen phosphorylase
Displaying 1 entry
Gene ID Gene Symbol Description Source
856289 GPH1 glycogen phosphorylase
The Human Phenotype Ontology
Displaying entries 31 - 32 of 32 in total
HPO ID HPO Term
HP:0008897 Postnatal growth retardation
HP:0000007 Autosomal recessive inheritance
Displaying 1 entry
Gene ID Gene Symbol Description
5836 PYGL glycogen phosphorylase L

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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Last updated: August 19, 2024