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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 ▲ |
|---|---|---|---|---|---|
| C0026266 | Mitral Valve Insufficiency | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C0432272 | Van Buchem disease | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C0011854 | Diabetes Mellitus, Insulin-Dependent | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C0158761 | Radioulnar Synostosis | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C0019270 | Hernia | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C0030409 | Paracoccidioidomycosis | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C0016522 | Foramen Ovale, Patent | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C0036341 | Schizophrenia | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C0008497 | Choriocarcinoma | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C2745959 | Spondyloepiphyseal dysplasia, congenita | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C0206686 | Adrenocortical carcinoma | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C0175778 | Larsen syndrome | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C0085083 | Ovarian Hyperstimulation Syndrome | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C0028754 | Obesity | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C0002418 | Amblyopia | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C0221356 | Brachycephaly | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C0036391 | Schwartz-Jampel Syndrome | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C0011849 | Diabetes Mellitus | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C4551479 | Schwartz-Jampel Syndrome, Type 1 | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C0878544 | Cardiomyopathies | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C0018818 | Ventricular Septal Defects | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C3203102 | Idiopathic pulmonary arterial hypertension | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C0003504 | Aortic Valve Insufficiency | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C0001624 | Adrenal Gland Neoplasms | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C0026760 | Multiple Epiphyseal Dysplasia | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
