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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 |
|---|---|---|---|---|---|
| C0220726 | Diastrophic dysplasia | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0029422 | Osteochondrodysplasias | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C3495559 | Juvenile arthritis | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0025500 | Mesothelioma | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0026760 | Multiple Epiphyseal Dysplasia | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C1306459 | Primary malignant neoplasm | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0013604 | Edema | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0016057 | Fibrosarcoma | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0031900 | Pierre Robin Syndrome | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0026650 | Movement Disorders | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0037926 | Compression of spinal cord | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0265283 | Atelosteogenesis, type 1 | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0015934 | Fetal Growth Retardation | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0001079 | Achondrogenesis | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0699790 | Colon Carcinoma | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0023075 | Laryngostenosis | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0020224 | Polyhydramnios | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0206620 | Lymphangioma, Cystic | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0027651 | Neoplasms | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0036439 | Scoliosis, unspecified | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0009081 | Congenital clubfoot | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0007131 | Non-Small Cell Lung Carcinoma | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0014179 | Endometritis | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0024623 | Malignant neoplasm of stomach | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0029464 | Osteosclerosis | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
