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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Gerstmann-Straussler-Scheinker syndrome
Summary
- Synonym
-
- Gerstmann-Straussler-Scheinker disease
- PRION DEMENTIA
- Definition
- A prion disease characterized by adult onset of memory loss, dementia, ataxia, and pathologic deposition of amyloid-like plaques in the brain.
- Super Class
- prion disease
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| O43451 | Maltase-glucoamylase | |
| P04156 | Major prion protein | |
| P06737 | Glycogen phosphorylase, liver form | |
| P07741 | Adenine phosphoribosyltransferase | |
| P11217 | Glycogen phosphorylase, muscle form | |
| P14410 | Sucrase-isomaltase, intestinal | |
| P22303 | Acetylcholinesterase | |
| P35575 | Glucose-6-phosphatase catalytic subunit 1 | |
| P40925 | Malate dehydrogenase, cytoplasmic | |
| P46976 | Glycogenin-1 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001315 | Reduced tendon reflexes |
| HP:0100543 | Cognitive impairment |
| HP:0002062 | Abnormal pyramidal tract morphology |
| HP:0001268 | Mental deterioration |
| HP:0003401 | Paresthesia |
| HP:0001824 | Weight loss |
| HP:0001257 | Spasticity |
| HP:0002354 | Memory impairment |
| HP:0000716 | Depression |
| HP:0002070 | Limb ataxia |
