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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Creutzfeldt-Jakob disease
Summary
- Synonym
-
- CJD
- Creutzfeldt Jacob syndrome
- Creutzfeldt Jakob disease
- Creutzfeldt-Jacob disease
- Jakob-Creutzfeldt disease
- Subacute spongiform encephalopathy
- Transmissible virus dementia
- Super Class
- prion disease
External Links
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 5293 | PIK3CD | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | |
| 5294 | PIK3CG | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | |
| 5310 | PKD1 | polycystin 1, transient receptor potential channel interacting | |
| 5336 | PLCG2 | phospholipase C gamma 2 | |
| 5621 | PRNP | prion protein (Kanno blood group) | |
| 5742 | PTGS1 | prostaglandin-endoperoxide synthase 1 | |
| 5743 | PTGS2 | prostaglandin-endoperoxide synthase 2 | |
| 6517 | SLC2A4 | solute carrier family 2 member 4 | |
| 6783 | SULT1E1 | sulfotransferase family 1E member 1 | |
| 7167 | TPI1 | triosephosphate isomerase 1 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P17931 | Galectin-3 | |
| P18669 | Phosphoglycerate mutase 1 | |
| P20138 | Myeloid cell surface antigen CD33 | |
| P22033 | Methylmalonyl-CoA mutase, mitochondrial | |
| P22303 | Acetylcholinesterase | |
| P23219 | Prostaglandin G/H synthase 1 | |
| P35354 | Prostaglandin G/H synthase 2 | |
| P35475 | Alpha-L-iduronidase | |
| P36222 | Chitinase-3-like protein 1 | |
| P40925 | Malate dehydrogenase, cytoplasmic |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0003487 | Babinski sign |
| HP:0005327 | Loss of facial expression |
| HP:0006943 | Diffuse spongiform leukoencephalopathy |
| HP:0007009 | Central nervous system degeneration |
| HP:0007017 | Progressive forgetfulness |
| HP:0007158 | Progressive extrapyramidal muscular rigidity |
| HP:0007183 | Focal T2 hyperintense basal ganglia lesion |
| HP:0007256 | Abnormal pyramidal sign |
| HP:0007686 | Abnormal pupillary function |
| HP:0010542 | Vestibular nystagmus |
