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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 |
|---|---|---|---|---|---|
| C0036572 | Seizures | PRNP | 5621 | prion protein | P04156 |
| C0011884 | Diabetic Retinopathy | PRNP | 5621 | prion protein | P04156 |
| C0040997 | Trigeminal Neuralgia | PRNP | 5621 | prion protein | P04156 |
| C0028841 | Ocular Hypotension | PRNP | 5621 | prion protein | P04156 |
| C3495559 | Juvenile arthritis | PRNP | 5621 | prion protein | P04156 |
| C0021400 | Influenza | PRNP | 5621 | prion protein | P04156 |
| C0007760 | Cerebellar Diseases | PRNP | 5621 | prion protein | P04156 |
| C0393911 | Pure Autonomic Failure | PRNP | 5621 | prion protein | P04156 |
| C0235974 | Pancreatic carcinoma | PRNP | 5621 | prion protein | P04156 |
| C0031117 | Peripheral Neuropathy | PRNP | 5621 | prion protein | P04156 |
| C0027126 | Myotonic Dystrophy | PRNP | 5621 | prion protein | P04156 |
| C0751785 | Unverricht-Lundborg Syndrome | PRNP | 5621 | prion protein | P04156 |
| C0025202 | melanoma | PRNP | 5621 | prion protein | P04156 |
| C0263912 | Rotator cuff syndrome | PRNP | 5621 | prion protein | P04156 |
| C0011269 | Dementia, Vascular | PRNP | 5621 | prion protein | P04156 |
| C0677886 | Epithelial ovarian cancer | PRNP | 5621 | prion protein | P04156 |
| C0033578 | Prostatic Neoplasms | PRNP | 5621 | prion protein | P04156 |
| C0033975 | Psychotic Disorders | PRNP | 5621 | prion protein | P04156 |
| C1839259 | Bulbo-Spinal Atrophy, X-Linked | PRNP | 5621 | prion protein | P04156 |
| C2750737 | DIARRHEA 5, WITH TUFTING ENTEROPATHY, CONGENITAL | PRNP | 5621 | prion protein | P04156 |
| C0038356 | Stomach Neoplasms | PRNP | 5621 | prion protein | P04156 |
| C3805618 | CEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED | PRNP | 5621 | prion protein | P04156 |
| C0233794 | Memory impairment | PRNP | 5621 | prion protein | P04156 |
| C0006111 | Brain Diseases | PRNP | 5621 | prion protein | P04156 |
| C0025289 | Meningitis | PRNP | 5621 | prion protein | P04156 |
