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DisGeNET
DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.
| Source | Last Updated |
|---|---|
| DisGeNET | July 29, 2024 |
| Disease ID | Disease Name | Gene Symbol ▲ | Gene ID | Gene Name | UniProt ID |
|---|---|---|---|---|---|
| C0206042 | Fatal Familial Insomnia | PRNP | 5621 | prion protein | P04156 |
| C0022336 | Creutzfeldt-Jakob disease | PRNP | 5621 | prion protein | P04156 |
| C0002726 | Amyloidosis | PRNP | 5621 | prion protein | P04156 |
| C0027888 | Hereditary Motor and Sensory Neuropathies | PRNP | 5621 | prion protein | P04156 |
| C1864112 | HUNTINGTON DISEASE-LIKE 1 | PRNP | 5621 | prion protein | P04156 |
| C0376329 | New Variant Creutzfeldt-Jakob Disease | PRNP | 5621 | prion protein | P04156 |
| C0007758 | Cerebellar Ataxia | PRNP | 5621 | prion protein | P04156 |
| C0376358 | Malignant neoplasm of prostate | PRNP | 5621 | prion protein | P04156 |
| C0022802 | Kuru | PRNP | 5621 | prion protein | P04156 |
| C1561643 | Chronic Kidney Diseases | PRNP | 5621 | prion protein | P04156 |
| C0343641 | Human papilloma virus infection | PRNP | 5621 | prion protein | P04156 |
| C0009402 | Colorectal Carcinoma | PRNP | 5621 | prion protein | P04156 |
| C0027651 | Neoplasms | PRNP | 5621 | prion protein | P04156 |
| C0497327 | Dementia | PRNP | 5621 | prion protein | P04156 |
| C0442874 | Neuropathy | PRNP | 5621 | prion protein | P04156 |
| C0027819 | Neuroblastoma | PRNP | 5621 | prion protein | P04156 |
| C4281802 | Spongiform encephalopathy | PRNP | 5621 | prion protein | P04156 |
| C0085584 | Encephalopathies | PRNP | 5621 | prion protein | P04156 |
| C0700095 | Central neuroblastoma | PRNP | 5621 | prion protein | P04156 |
| C0751781 | Dentatorubral-Pallidoluysian Atrophy | PRNP | 5621 | prion protein | P04156 |
| C1621958 | Glioblastoma Multiforme | PRNP | 5621 | prion protein | P04156 |
| C1335302 | Pancreatic Ductal Adenocarcinoma | PRNP | 5621 | prion protein | P04156 |
| C0004114 | Astrocytoma | PRNP | 5621 | prion protein | P04156 |
| C0011265 | Presenile dementia | PRNP | 5621 | prion protein | P04156 |
| C0270911 | Charcot-Marie-Tooth Disease, Type Ia (disorder) | PRNP | 5621 | prion protein | P04156 |
