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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 ▲ |
|---|---|---|---|---|---|
| C0017658 | Glomerulonephritis | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0004238 | Atrial Fibrillation | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0006826 | Malignant Neoplasms | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C1384666 | hearing impairment | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0007786 | Brain Ischemia | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0022658 | Kidney Diseases | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0004153 | Atherosclerosis | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C1862941 | Amyotrophic Lateral Sclerosis, Sporadic | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0796074 | MOHR-TRANEBJAERG SYNDROME | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0007785 | Cerebral Infarction | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C4551858 | Vesicoureteral Reflux 1 | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0376358 | Malignant neoplasm of prostate | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0014547 | Epilepsies, Partial | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0155616 | Secondary hypertension | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C1956346 | Coronary Artery Disease | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0002395 | Alzheimer's Disease | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0086543 | Cataract | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0038454 | Cerebrovascular accident | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0007194 | Hypertrophic Cardiomyopathy | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0024796 | Marfan Syndrome | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0206624 | Hepatoblastoma | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0011581 | Depressive disorder | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0001430 | Adenoma | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0037772 | Spastic Paraplegia | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0010054 | Coronary Arteriosclerosis | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
