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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 |
|---|---|---|---|---|---|
| C0029408 | Degenerative polyarthritis | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0409959 | Osteoarthritis, Knee | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C1306503 | Congenital exomphalos | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0029456 | Osteoporosis | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C1857255 | Diastrophic Dysplasia, Broad Bone-Platyspondylic Variant | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0007102 | Malignant tumor of colon | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0013336 | Dwarfism | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0038018 | Spondylolysis | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0006142 | Malignant neoplasm of breast | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0392476 | Epiphyseal dysplasia | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0025517 | Metabolic Diseases | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0271829 | Pendred's syndrome | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0019294 | Hernia, Inguinal | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0022104 | Irritable Bowel Syndrome | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0699791 | Stomach Carcinoma | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0008925 | Cleft Palate | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C1384514 | Conn Syndrome | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0026707 | Mucopolysaccharidosis IV | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0024121 | Lung Neoplasms | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0013447 | Ear Diseases | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0024894 | Mastitis | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0001430 | Adenoma | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0011991 | Diarrhea | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0575158 | Kyphoscoliosis deformity of spine | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
| C0029899 | Otosclerosis | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
