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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 |
|---|---|---|---|---|---|
| C1140680 | Malignant neoplasm of ovary | STS | 412 | steroid sulfatase | P08842 |
| C0028738 | Nystagmus | STS | 412 | steroid sulfatase | P08842 |
| C2931498 | Mental Retardation, X-Linked 1 | STS | 412 | steroid sulfatase | P08842 |
| C0020758 | Congenital ichthyosis | STS | 412 | steroid sulfatase | P08842 |
| C0008354 | Cholera | STS | 412 | steroid sulfatase | P08842 |
| C0007847 | Malignant tumor of cervix | STS | 412 | steroid sulfatase | P08842 |
| C0600139 | Prostate carcinoma | STS | 412 | steroid sulfatase | P08842 |
| C0278878 | Adult Glioblastoma | STS | 412 | steroid sulfatase | P08842 |
| C0024623 | Malignant neoplasm of stomach | STS | 412 | steroid sulfatase | P08842 |
| C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | STS | 412 | steroid sulfatase | P08842 |
| C1458155 | Mammary Neoplasms | STS | 412 | steroid sulfatase | P08842 |
| C0019196 | Hepatitis C | STS | 412 | steroid sulfatase | P08842 |
| C0008445 | Chondrodysplasia Punctata | STS | 412 | steroid sulfatase | P08842 |
| C0003873 | Rheumatoid Arthritis | STS | 412 | steroid sulfatase | P08842 |
| C3714756 | Intellectual Disability | STS | 412 | steroid sulfatase | P08842 |
| C0333875 | High-Grade Squamous Intraepithelial Lesions | STS | 412 | steroid sulfatase | P08842 |
| C0264408 | Childhood asthma | STS | 412 | steroid sulfatase | P08842 |
| C0343641 | Human papilloma virus infection | STS | 412 | steroid sulfatase | P08842 |
| C0751955 | Brain Infarction | STS | 412 | steroid sulfatase | P08842 |
| C0206698 | Cholangiocarcinoma | STS | 412 | steroid sulfatase | P08842 |
| C0699885 | Carcinoma of bladder | STS | 412 | steroid sulfatase | P08842 |
| C0262584 | Carcinoma, Small Cell | STS | 412 | steroid sulfatase | P08842 |
| C1848638 | USHER SYNDROME, TYPE IB (disorder) | STS | 412 | steroid sulfatase | P08842 |
| C2711227 | Steatohepatitis | STS | 412 | steroid sulfatase | P08842 |
| C1510586 | Autism Spectrum Disorders | STS | 412 | steroid sulfatase | P08842 |
