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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 |
|---|---|---|---|---|---|
| C0700095 | Central neuroblastoma | PRNP | 5621 | prion protein | F7VJQ1 |
| C0751781 | Dentatorubral-Pallidoluysian Atrophy | PRNP | 5621 | prion protein | F7VJQ1 |
| C1621958 | Glioblastoma Multiforme | PRNP | 5621 | prion protein | F7VJQ1 |
| C1335302 | Pancreatic Ductal Adenocarcinoma | PRNP | 5621 | prion protein | F7VJQ1 |
| C0004114 | Astrocytoma | PRNP | 5621 | prion protein | F7VJQ1 |
| C0011265 | Presenile dementia | PRNP | 5621 | prion protein | F7VJQ1 |
| C0270911 | Charcot-Marie-Tooth Disease, Type Ia (disorder) | PRNP | 5621 | prion protein | F7VJQ1 |
| C0346647 | Malignant neoplasm of pancreas | PRNP | 5621 | prion protein | F7VJQ1 |
| C1319315 | Adenocarcinoma of large intestine | PRNP | 5621 | prion protein | F7VJQ1 |
| C0276496 | Familial Alzheimer Disease (FAD) | PRNP | 5621 | prion protein | F7VJQ1 |
| C0751254 | Creutzfeldt-Jakob Disease, Familial | PRNP | 5621 | prion protein | F7VJQ1 |
| C0340978 | May-Hegglin anomaly | PRNP | 5621 | prion protein | F7VJQ1 |
| C1135993 | Wasting Disease, Chronic | PRNP | 5621 | prion protein | F7VJQ1 |
| C0023524 | Leukoencephalopathy, Progressive Multifocal | PRNP | 5621 | prion protein | F7VJQ1 |
| C0015934 | Fetal Growth Retardation | PRNP | 5621 | prion protein | F7VJQ1 |
| C0000768 | Congenital Abnormality | PRNP | 5621 | prion protein | F7VJQ1 |
| C0017636 | Glioblastoma | PRNP | 5621 | prion protein | F7VJQ1 |
| C0041696 | Unipolar Depression | PRNP | 5621 | prion protein | F7VJQ1 |
| C1306459 | Primary malignant neoplasm | PRNP | 5621 | prion protein | F7VJQ1 |
| C0339573 | Glaucoma, Primary Open Angle | PRNP | 5621 | prion protein | F7VJQ1 |
| C0006826 | Malignant Neoplasms | PRNP | 5621 | prion protein | F7VJQ1 |
| C0003635 | Apraxias | PRNP | 5621 | prion protein | F7VJQ1 |
| C0038644 | Sudden infant death syndrome | PRNP | 5621 | prion protein | F7VJQ1 |
| C0021390 | Inflammatory Bowel Diseases | PRNP | 5621 | prion protein | F7VJQ1 |
| C0028754 | Obesity | PRNP | 5621 | prion protein | F7VJQ1 |
