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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 ▲ |
|---|---|---|---|---|---|
| C0032897 | Prader-Willi Syndrome | PRNP | 5621 | prion protein | P04156 |
| C0035334 | Retinitis Pigmentosa | PRNP | 5621 | prion protein | P04156 |
| C1168401 | Squamous cell carcinoma of the head and neck | PRNP | 5621 | prion protein | P04156 |
| C0005586 | Bipolar Disorder | PRNP | 5621 | prion protein | P04156 |
| C0007134 | Renal Cell Carcinoma | PRNP | 5621 | prion protein | P04156 |
| C1378703 | Renal carcinoma | PRNP | 5621 | prion protein | P04156 |
| C0027809 | Neurilemmoma | PRNP | 5621 | prion protein | P04156 |
| C0751782 | May-White Syndrome | PRNP | 5621 | prion protein | P04156 |
| C0751780 | Biotin-Responsive Encephalopathy | PRNP | 5621 | prion protein | P04156 |
| C1531647 | Cerebral ventriculomegaly | PRNP | 5621 | prion protein | P04156 |
| C0007097 | Carcinoma | PRNP | 5621 | prion protein | P04156 |
| C0007682 | CNS disorder | PRNP | 5621 | prion protein | P04156 |
| C0042900 | Vitiligo | PRNP | 5621 | prion protein | P04156 |
| C0020538 | Hypertensive disease | PRNP | 5621 | prion protein | P04156 |
| C0917799 | Hypersomnia | PRNP | 5621 | prion protein | P04156 |
| C0020456 | Hyperglycemia | PRNP | 5621 | prion protein | P04156 |
| C0242379 | Malignant neoplasm of lung | PRNP | 5621 | prion protein | P04156 |
| C0007137 | Squamous cell carcinoma | PRNP | 5621 | prion protein | P04156 |
| C0268398 | Familial lichen amyloidosis | PRNP | 5621 | prion protein | P04156 |
| C0042769 | Virus Diseases | PRNP | 5621 | prion protein | P04156 |
| C1835614 | Hereditary Hyperexplexia | PRNP | 5621 | prion protein | P04156 |
| C0520966 | Abnormal coordination | PRNP | 5621 | prion protein | P04156 |
| C4721610 | Carcinoma, Ovarian Epithelial | PRNP | 5621 | prion protein | P04156 |
| C0751777 | Familial Progressive Myoclonic Epilepsy | PRNP | 5621 | prion protein | P04156 |
| C0004138 | Ataxias, Hereditary | PRNP | 5621 | prion protein | P04156 |
