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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 |
|---|---|---|---|---|---|
| C0007102 | Malignant tumor of colon | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0006826 | Malignant Neoplasms | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0014474 | Ependymoma | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0278876 | Adult Medulloblastoma | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C1306459 | Primary malignant neoplasm | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0007114 | Malignant neoplasm of skin | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0026764 | Multiple Myeloma | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0699790 | Colon Carcinoma | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0027651 | Neoplasms | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0740345 | Germ Cell Cancer | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0346647 | Malignant neoplasm of pancreas | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0019163 | Hepatitis B | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0006142 | Malignant neoplasm of breast | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0678222 | Breast Carcinoma | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C0235974 | Pancreatic carcinoma | TDG | 6996 | thymine DNA glycosylase | Q13569 |
| C1866095 | Deafness, Autosomal Dominant 13 | TECTA | 7007 | tectorin alpha | O75443 |
| C1384666 | hearing impairment | TECTA | 7007 | tectorin alpha | O75443 |
| C1857276 | Trichohepatoenteric Syndrome | TECTA | 7007 | tectorin alpha | O75443 |
| C1832187 | Deafness, Autosomal Dominant 12 | TECTA | 7007 | tectorin alpha | O75443 |
| C0339789 | Congenital deafness | TECTA | 7007 | tectorin alpha | O75443 |
| C2020284 | Stickler syndrome, type 1 | TECTA | 7007 | tectorin alpha | O75443 |
| C0018780 | Hearing Loss, High-Frequency | TECTA | 7007 | tectorin alpha | O75443 |
| C0011053 | Deafness | TECTA | 7007 | tectorin alpha | O75443 |
| C0018784 | Sensorineural Hearing Loss (disorder) | TECTA | 7007 | tectorin alpha | O75443 |
| C0019360 | Herpes zoster disease | TECTA | 7007 | tectorin alpha | O75443 |
