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
Disease Ontology
DOID:2754
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
5836 PYGL glycogen phosphorylase L
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 21 - 30 of 32 in total
HPO ID HPO Term
HP:0002910 Elevated circulating hepatic transaminase concentration
HP:0011997 Postprandial hyperlactemia
HP:0000939 Osteoporosis
HP:0001943 Hypoglycemia
HP:0000093 Proteinuria
HP:0004322 Short stature
HP:0001395 Hepatic fibrosis
HP:0000007 Autosomal recessive inheritance
HP:0003124 Hypercholesterolemia
HP:0008897 Postnatal growth retardation
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

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


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Last updated: December 9, 2024