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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 ▲ |
|---|---|---|---|---|---|
| C0029408 | Degenerative polyarthritis | PRNP | 5621 | prion protein | F7VJQ1 |
| C0233844 | Clumsiness | PRNP | 5621 | prion protein | F7VJQ1 |
| C4721453 | Peripheral Nervous System Diseases | PRNP | 5621 | prion protein | F7VJQ1 |
| C0525045 | Mood Disorders | PRNP | 5621 | prion protein | F7VJQ1 |
| C0751956 | Acute Cerebrovascular Accidents | PRNP | 5621 | prion protein | F7VJQ1 |
| C0008489 | Chorea | PRNP | 5621 | prion protein | F7VJQ1 |
| C0684249 | Carcinoma of lung | PRNP | 5621 | prion protein | F7VJQ1 |
| C0001175 | Acquired Immunodeficiency Syndrome | PRNP | 5621 | prion protein | F7VJQ1 |
| C0017638 | Glioma | PRNP | 5621 | prion protein | F7VJQ1 |
| C0038868 | Progressive supranuclear palsy | PRNP | 5621 | prion protein | F7VJQ1 |
| C0751494 | Convulsive Seizures | PRNP | 5621 | prion protein | F7VJQ1 |
| C0751713 | Inclusion Body Myopathy, Sporadic | PRNP | 5621 | prion protein | F7VJQ1 |
| C0007785 | Cerebral Infarction | PRNP | 5621 | prion protein | F7VJQ1 |
| C0259749 | Autonomic neuropathy | PRNP | 5621 | prion protein | F7VJQ1 |
| C0029463 | Osteosarcoma | PRNP | 5621 | prion protein | F7VJQ1 |
| C0032897 | Prader-Willi Syndrome | PRNP | 5621 | prion protein | F7VJQ1 |
| C0035334 | Retinitis Pigmentosa | PRNP | 5621 | prion protein | F7VJQ1 |
| C1168401 | Squamous cell carcinoma of the head and neck | PRNP | 5621 | prion protein | F7VJQ1 |
| C0005586 | Bipolar Disorder | PRNP | 5621 | prion protein | F7VJQ1 |
| C0007134 | Renal Cell Carcinoma | PRNP | 5621 | prion protein | F7VJQ1 |
| C1378703 | Renal carcinoma | PRNP | 5621 | prion protein | F7VJQ1 |
| C0027809 | Neurilemmoma | PRNP | 5621 | prion protein | F7VJQ1 |
| C0751782 | May-White Syndrome | PRNP | 5621 | prion protein | F7VJQ1 |
| C0751780 | Biotin-Responsive Encephalopathy | PRNP | 5621 | prion protein | F7VJQ1 |
| C1531647 | Cerebral ventriculomegaly | PRNP | 5621 | prion protein | F7VJQ1 |
