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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 |
|---|---|---|---|---|---|
| C0019196 | Hepatitis C | PRNP | 5621 | prion protein | P04156 |
| C0027765 | nervous system disorder | PRNP | 5621 | prion protein | P04156 |
| C0019163 | Hepatitis B | PRNP | 5621 | prion protein | P04156 |
| C0002736 | Amyotrophic Lateral Sclerosis | PRNP | 5621 | prion protein | P04156 |
| C0585442 | Osteosarcoma of bone | PRNP | 5621 | prion protein | P04156 |
| C2931022 | Amyloidosis, Cerebral, with Spongiform Encephalopathy | PRNP | 5621 | prion protein | P04156 |
| C0349081 | Dementia in Parkinson's disease | PRNP | 5621 | prion protein | P04156 |
| C0036457 | Scrapie | PRNP | 5621 | prion protein | P04156 |
| C1568272 | Tendinopathy | PRNP | 5621 | prion protein | P04156 |
| C0282513 | Primary Progressive Aphasia (disorder) | PRNP | 5621 | prion protein | P04156 |
| C0014038 | Encephalitis | PRNP | 5621 | prion protein | P04156 |
| C1263846 | Attention deficit hyperactivity disorder | PRNP | 5621 | prion protein | P04156 |
| C0027066 | Myoclonus | PRNP | 5621 | prion protein | P04156 |
| C0409959 | Osteoarthritis, Knee | PRNP | 5621 | prion protein | P04156 |
| C0752125 | Spinocerebellar Ataxia Type 7 | PRNP | 5621 | prion protein | P04156 |
| C0005129 | Bernard-Soulier Syndrome | PRNP | 5621 | prion protein | P04156 |
| C0036341 | Schizophrenia | PRNP | 5621 | prion protein | P04156 |
| C0030567 | Parkinson Disease | PRNP | 5621 | prion protein | P04156 |
| C0949664 | Tauopathies | PRNP | 5621 | prion protein | P04156 |
| C0752347 | Lewy Body Disease | PRNP | 5621 | prion protein | P04156 |
| C0014556 | Epilepsy, Temporal Lobe | PRNP | 5621 | prion protein | P04156 |
| C0024790 | Paroxysmal nocturnal hemoglobinuria | PRNP | 5621 | prion protein | P04156 |
| C0026848 | Myopathy | PRNP | 5621 | prion protein | P04156 |
| C3665347 | Visual Impairment | PRNP | 5621 | prion protein | P04156 |
| C0393547 | Bulbospinal Neuronopathy | PRNP | 5621 | prion protein | P04156 |
