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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
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 6120 | RPE | ribulose-5-phosphate-3-epimerase | |
| 6476 | SI | sucrase-isomaltase | |
| 6785 | ELOVL4 | ELOVL fatty acid elongase 4 | |
| 8972 | MGAM | maltase-glucoamylase | |
| 8987 | STBD1 | starch binding domain 1 | |
| 10159 | ATP6AP2 | ATPase H+ transporting accessory protein 2 | |
| 10327 | AKR1A1 | aldo-keto reductase family 1 member A1 | |
| 26503 | SLC17A5 | solute carrier family 17 member 5 | |
| 27306 | HPGDS | hematopoietic prostaglandin D synthase | |
| 54575 | UGT1A10 | UDP glucuronosyltransferase family 1 member A10 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P22310 | UDP-glucuronosyltransferase 1A4 | |
| P23786 | Carnitine O-palmitoyltransferase 2, mitochondrial | |
| P27797 | Calreticulin | |
| P35475 | Alpha-L-iduronidase | |
| P35503 | UDP-glucuronosyltransferase 1A3 | |
| P35504 | UDP-glucuronosyltransferase 1A5 | |
| P35573 | Glycogen debranching enzyme | |
| P35575 | Glucose-6-phosphatase catalytic subunit 1 | |
| P46976 | Glycogenin-1 | |
| P54803 | Galactocerebrosidase |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0003690 | Limb muscle weakness |
| HP:0001945 | Fever |
| HP:0000020 | Urinary incontinence |
| HP:0003725 | Firm muscles |
| HP:0001716 | Wolff-Parkinson-White syndrome |
| HP:0009051 | Increased muscle glycogen content |
| HP:0002094 | Dyspnea |
| HP:0001265 | Hyporeflexia |
| HP:0003546 | Exercise intolerance |
| HP:0000007 | Autosomal recessive inheritance |
