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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 |
|---|---|---|---|---|---|
| C1306459 | Primary malignant neoplasm | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0279628 | Adenocarcinoma Of Esophagus | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0678222 | Breast Carcinoma | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0085584 | Encephalopathies | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0002878 | Anemia, Hemolytic | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0036439 | Scoliosis, unspecified | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0005684 | Malignant neoplasm of urinary bladder | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0020490 | Hyperopia | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0684276 | Hypsarrhythmia | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0282577 | Congenital Disorders of Glycosylation | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0020615 | Hypoglycemia | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0947622 | Cholecystolithiasis | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C1332979 | Childhood Lymphoma | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0025958 | Microcephaly | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0037769 | West Syndrome | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0024299 | Lymphoma | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0546837 | Malignant neoplasm of esophagus | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0023895 | Liver diseases | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C1636149 | Macular dystrophy, corneal type 1 | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0002395 | Alzheimer's Disease | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0002875 | Cooley's anemia | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C1527366 | Salaam Seizures | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0014859 | Esophageal Neoplasms | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0221023 | Cyclic neutropenia | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0152018 | Esophageal carcinoma | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
