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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 |
|---|---|---|---|
| 3482 | IGF2R | insulin like growth factor 2 receptor | |
| 3635 | INPP5D | inositol polyphosphate-5-phosphatase D | |
| 3958 | LGALS3 | galectin 3 | |
| 4190 | MDH1 | malate dehydrogenase 1 | |
| 4594 | MMUT | methylmalonyl-CoA mutase | |
| 4684 | NCAM1 | neural cell adhesion molecule 1 | |
| 4967 | OGDH | oxoglutarate dehydrogenase | |
| 5223 | PGAM1 | phosphoglycerate mutase 1 | |
| 5290 | PIK3CA | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | |
| 5291 | PIK3CB | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta |
Related Glycoprotein
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001269 | Hemiparesis |
| HP:0000505 | Visual impairment |
| HP:0002381 | Aphasia |
| HP:0001317 | Abnormal cerebellum morphology |
| HP:0000006 | Autosomal dominant inheritance |
| HP:0002354 | Memory impairment |
| HP:0003678 | Rapidly progressive |
| HP:0007076 | Extrapyramidal muscular rigidity |
