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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 |
|---|---|---|---|---|---|
| C0020503 | Hyperparathyroidism, Secondary | UMOD | 7369 | uromodulin | P07911 |
| C0282488 | Interstitial Cystitis | UMOD | 7369 | uromodulin | P07911 |
| C0023452 | Childhood Acute Lymphoblastic Leukemia | UMOD | 7369 | uromodulin | P07911 |
| C0948008 | Ischemic stroke | UMOD | 7369 | uromodulin | P07911 |
| C0005684 | Malignant neoplasm of urinary bladder | UMOD | 7369 | uromodulin | P07911 |
| C1332977 | Childhood Leukemia | UMOD | 7369 | uromodulin | P07911 |
| C0085548 | Autosomal Recessive Polycystic Kidney Disease | UMOD | 7369 | uromodulin | P07911 |
| C0024138 | Lupus Erythematosus, Discoid | UMOD | 7369 | uromodulin | P07911 |
| C0010346 | Crohn Disease | UST | 10090 | uronyl 2-sulfotransferase | Q9Y2C2 |
| C0038013 | Ankylosing spondylitis | UST | 10090 | uronyl 2-sulfotransferase | Q9Y2C2 |
| C0006826 | Malignant Neoplasms | UST | 10090 | uronyl 2-sulfotransferase | Q9Y2C2 |
| C0004238 | Atrial Fibrillation | UST | 10090 | uronyl 2-sulfotransferase | Q9Y2C2 |
| C0235480 | Paroxysmal atrial fibrillation | UST | 10090 | uronyl 2-sulfotransferase | Q9Y2C2 |
| C0269102 | Endometrioma | UST | 10090 | uronyl 2-sulfotransferase | Q9Y2C2 |
| C0029408 | Degenerative polyarthritis | UST | 10090 | uronyl 2-sulfotransferase | Q9Y2C2 |
| C0014175 | Endometriosis | UST | 10090 | uronyl 2-sulfotransferase | Q9Y2C2 |
| C0033860 | Psoriasis | VNN1 | 8876 | vanin 1 | O95497 |
| C0025517 | Metabolic Diseases | VNN1 | 8876 | vanin 1 | O95497 |
| C0015624 | Fanconi Syndrome | VNN1 | 8876 | vanin 1 | O95497 |
| C1306459 | Primary malignant neoplasm | VNN1 | 8876 | vanin 1 | O95497 |
| C0009402 | Colorectal Carcinoma | VNN1 | 8876 | vanin 1 | O95497 |
| C0178664 | Glomerulosclerosis (disorder) | VNN1 | 8876 | vanin 1 | O95497 |
| C0149939 | Obstructive nephropathy | VNN1 | 8876 | vanin 1 | O95497 |
| C0004153 | Atherosclerosis | VNN1 | 8876 | vanin 1 | O95497 |
| C0699790 | Colon Carcinoma | VNN1 | 8876 | vanin 1 | O95497 |
