glycogen storage disease II

Summary
Synonym
  • Generalized glycogenosis
  • Glycogen storage disease 2
  • Glycogen storage disease, type II
  • Glycogenosis, type 2
  • Lysosomal alpha-1,4-glucosidase deficiency
  • Pompe's disease
  • acid maltase deficiency
  • deficiency of glucoamylase
  • deficiency of maltase
  • glycogen storage disease type II
Definition
A glycogen storage disease that has_material_basis_in deficiency of the lysosomal acid alpha-glucosidase enzyme resulting in damage to muscle and nerve cells due to an accumulation of glycogen in the lysosome.
Super Class
autosomal recessive disease glycogen storage disease
External Links
Disease Ontology
DOID:2752
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying entries 1 - 10 of 39 in total
Gene ID Gene Symbol Description Source
142 PARP1 poly(ADP-ribose) polymerase 1
178 AGL amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase
353 APRT adenine phosphoribosyltransferase
411 ARSB arylsulfatase B
811 CALR calreticulin
1376 CPT2 carnitine palmitoyltransferase 2
1636 ACE angiotensin I converting enzyme
2215 FCGR3B Fc gamma receptor IIIb
2523 FUT1 fucosyltransferase 1 (H blood group)
2538 G6PC1 glucose-6-phosphatase catalytic subunit 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
14387 Gaa glucosidase, alpha, acid
Displaying 1 entry
Gene ID Gene Symbol Description Source
367562 Gaa alpha glucosidase
The Human Phenotype Ontology
Displaying entries 41 - 50 of 50 in total
HPO ID HPO Term
HP:0002355 Difficulty walking
HP:0004944 Dilatation of the cerebral artery
HP:0001744 Splenomegaly
HP:0011400 Abnormal CNS myelination
HP:0002138 Subarachnoid hemorrhage
HP:0003551 Difficulty climbing stairs
HP:0011703 Sinus tachycardia
HP:0002205 Recurrent respiratory infections
HP:0001252 Hypotonia
HP:0006597 Diaphragmatic paralysis
Displaying 1 entry
Gene ID Gene Symbol Description
2548 GAA alpha glucosidase

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Last updated: August 19, 2024