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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 |
|---|---|---|---|---|---|
| C0014544 | Epilepsy | PRNP | 5621 | prion protein | F7VJQ1 |
| C0338451 | Frontotemporal dementia | PRNP | 5621 | prion protein | F7VJQ1 |
| C1853926 | NONAKA MYOPATHY | PRNP | 5621 | prion protein | F7VJQ1 |
| C0032027 | Pityriasis Rubra Pilaris | PRNP | 5621 | prion protein | F7VJQ1 |
| C0013080 | Down Syndrome | PRNP | 5621 | prion protein | F7VJQ1 |
| C0001418 | Adenocarcinoma | PRNP | 5621 | prion protein | F7VJQ1 |
| C0494463 | Alzheimer Disease, Late Onset | PRNP | 5621 | prion protein | F7VJQ1 |
| C0087012 | Ataxia, Spinocerebellar | PRNP | 5621 | prion protein | F7VJQ1 |
| C0750901 | Alzheimer Disease, Early Onset | PRNP | 5621 | prion protein | F7VJQ1 |
| C0152013 | Adenocarcinoma of lung (disorder) | PRNP | 5621 | prion protein | F7VJQ1 |
| C0008479 | Chondrosarcoma | PRNP | 5621 | prion protein | F7VJQ1 |
| C1867773 | CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 1 | PRNP | 5621 | prion protein | F7VJQ1 |
| C0020179 | Huntington Disease | PRNP | 5621 | prion protein | F7VJQ1 |
| C0019202 | Hepatolenticular Degeneration | PRNP | 5621 | prion protein | F7VJQ1 |
| C0019196 | Hepatitis C | PRNP | 5621 | prion protein | F7VJQ1 |
| C0027765 | nervous system disorder | PRNP | 5621 | prion protein | F7VJQ1 |
| C0019163 | Hepatitis B | PRNP | 5621 | prion protein | F7VJQ1 |
| C0002736 | Amyotrophic Lateral Sclerosis | PRNP | 5621 | prion protein | F7VJQ1 |
| C0585442 | Osteosarcoma of bone | PRNP | 5621 | prion protein | F7VJQ1 |
| C2931022 | Amyloidosis, Cerebral, with Spongiform Encephalopathy | PRNP | 5621 | prion protein | F7VJQ1 |
| C0349081 | Dementia in Parkinson's disease | PRNP | 5621 | prion protein | F7VJQ1 |
| C0036457 | Scrapie | PRNP | 5621 | prion protein | F7VJQ1 |
| C1568272 | Tendinopathy | PRNP | 5621 | prion protein | F7VJQ1 |
| C0282513 | Primary Progressive Aphasia (disorder) | PRNP | 5621 | prion protein | F7VJQ1 |
| C0014038 | Encephalitis | PRNP | 5621 | prion protein | F7VJQ1 |
