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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 |
|---|---|---|---|---|---|
| C0017601 | Glaucoma | PRNP | 5621 | prion protein | P04156 |
| C0001889 | Akinetic Mutism | PRNP | 5621 | prion protein | P04156 |
| C0002895 | Anemia, Sickle Cell | PRNP | 5621 | prion protein | P04156 |
| C0027051 | Myocardial Infarction | PRNP | 5621 | prion protein | P04156 |
| C0028738 | Nystagmus | PRNP | 5621 | prion protein | P04156 |
| C0038454 | Cerebrovascular accident | PRNP | 5621 | prion protein | P04156 |
| C1332986 | Childhood Osteosarcoma | PRNP | 5621 | prion protein | P04156 |
| C0162311 | Androgenetic Alopecia | PRNP | 5621 | prion protein | P04156 |
| C0017609 | Glaucoma, Neovascular | PRNP | 5621 | prion protein | P04156 |
| C0009806 | Constipation | PRNP | 5621 | prion protein | P04156 |
| C1969957 | Creutzfeldt-Jakob Disease, Heidenhain Variant | PRNP | 5621 | prion protein | P04156 |
| C0002170 | Alopecia | PRNP | 5621 | prion protein | P04156 |
| C0751772 | REM Sleep Behavior Disorder | PRNP | 5621 | prion protein | P04156 |
| C4083212 | Alopecia, Male Pattern | PRNP | 5621 | prion protein | P04156 |
| C0524851 | Neurodegenerative Disorders | PRNP | 5621 | prion protein | F7VJQ1 |
| C1852467 | Creutzfeldt-Jakob Disease, Sporadic | PRNP | 5621 | prion protein | F7VJQ1 |
| C0162534 | Prion Diseases | PRNP | 5621 | prion protein | F7VJQ1 |
| C0002395 | Alzheimer's Disease | PRNP | 5621 | prion protein | F7VJQ1 |
| C0006142 | Malignant neoplasm of breast | PRNP | 5621 | prion protein | F7VJQ1 |
| C0017495 | Gerstmann-Straussler-Scheinker Disease | PRNP | 5621 | prion protein | F7VJQ1 |
| C0026650 | Movement Disorders | PRNP | 5621 | prion protein | F7VJQ1 |
| C0206042 | Fatal Familial Insomnia | PRNP | 5621 | prion protein | F7VJQ1 |
| C0022336 | Creutzfeldt-Jakob disease | PRNP | 5621 | prion protein | F7VJQ1 |
| C0002726 | Amyloidosis | PRNP | 5621 | prion protein | F7VJQ1 |
| C0027888 | Hereditary Motor and Sensory Neuropathies | PRNP | 5621 | prion protein | F7VJQ1 |
