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 ▼ |
---|---|---|---|---|---|
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 |
C0024117 | Chronic Obstructive Airway Disease | PRNP | 5621 | prion protein | P04156 |
C0032002 | Pituitary Diseases | PRNP | 5621 | prion protein | P04156 |
C0003850 | Arteriosclerosis | PRNP | 5621 | prion protein | P04156 |
C0149931 | Migraine Disorders | PRNP | 5621 | prion protein | P04156 |
C1861736 | SPINOCEREBELLAR ATAXIA 31 (disorder) | PRNP | 5621 | prion protein | P04156 |
C0031069 | Familial Mediterranean Fever | PRNP | 5621 | prion protein | P04156 |
C0205710 | Alpers Syndrome (disorder) | PRNP | 5621 | prion protein | P04156 |
C1306600 | Radial nerve palsy | PRNP | 5621 | prion protein | P04156 |
C1708349 | Hereditary Diffuse Gastric Cancer | PRNP | 5621 | prion protein | P04156 |
C1854520 | SEBASTIAN SYNDROME | PRNP | 5621 | prion protein | P04156 |
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 |
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Last updated: August 19, 2024