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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 |
|---|---|---|---|---|---|
| C0009946 | Conversion disorder | PRNP | 5621 | prion protein | P04156 |
| C0242422 | Parkinsonian Disorders | PRNP | 5621 | prion protein | P04156 |
| C0278878 | Adult Glioblastoma | PRNP | 5621 | prion protein | P04156 |
| C1269683 | Major Depressive Disorder | PRNP | 5621 | prion protein | P04156 |
| C0004096 | Asthma | PRNP | 5621 | prion protein | P04156 |
| C1458155 | Mammary Neoplasms | PRNP | 5621 | prion protein | P04156 |
| C2239176 | Liver carcinoma | PRNP | 5621 | prion protein | P04156 |
| C0004153 | Atherosclerosis | PRNP | 5621 | prion protein | P04156 |
| C0003467 | Anxiety | PRNP | 5621 | prion protein | P04156 |
| C0751778 | Myoclonic Epilepsies, Progressive | PRNP | 5621 | prion protein | P04156 |
| C0019187 | Hepatitis, Alcoholic | PRNP | 5621 | prion protein | P04156 |
| C0155379 | Nystagmus associated with disorder of the vestibular system | PRNP | 5621 | prion protein | P04156 |
| C0751776 | Atypical Inclusion-Body Disease | PRNP | 5621 | prion protein | P04156 |
| C0011581 | Depressive disorder | PRNP | 5621 | prion protein | P04156 |
| C1285162 | Degenerative disorder | PRNP | 5621 | prion protein | P04156 |
| C0751779 | Action Myoclonus-Renal Failure Syndrome | PRNP | 5621 | prion protein | P04156 |
| C0020258 | Hydrocephalus, Normal Pressure | PRNP | 5621 | prion protein | P04156 |
| C0011311 | Dengue Fever | PRNP | 5621 | prion protein | P04156 |
| C0270922 | Peripheral demyelinating neuropathy | PRNP | 5621 | prion protein | P04156 |
| C0010674 | Cystic Fibrosis | PRNP | 5621 | prion protein | P04156 |
| C0019069 | Hemophilia A | PRNP | 5621 | prion protein | P04156 |
| C1857276 | Trichohepatoenteric Syndrome | PRNP | 5621 | prion protein | P04156 |
| C0751645 | Human Transmissible Spongiform Encephalopathies, Inherited | PRNP | 5621 | prion protein | P04156 |
| C0011991 | Diarrhea | PRNP | 5621 | prion protein | P04156 |
| C0007786 | Brain Ischemia | PRNP | 5621 | prion protein | P04156 |
