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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 |
|---|---|---|---|---|---|
| C0205644 | Carcinoma, Granular Cell | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0037773 | Spastic Paraplegia, Hereditary | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0028738 | Nystagmus | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0009324 | Ulcerative Colitis | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0023895 | Liver diseases | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0008372 | Intrahepatic Cholestasis | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0009402 | Colorectal Carcinoma | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0009714 | Hepatic Fibrosis, Congenital | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0086565 | Liver Dysfunction | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C2931356 | Spastic paraplegia type 5A, recessive | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0027651 | Neoplasms | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C1306459 | Primary malignant neoplasm | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0006826 | Malignant Neoplasms | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0376358 | Malignant neoplasm of prostate | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C1836230 | HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0005779 | Blood Coagulation Disorders | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C2711227 | Steatohepatitis | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0026769 | Multiple Sclerosis | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0003873 | Rheumatoid Arthritis | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0086543 | Cataract | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0524851 | Neurodegenerative Disorders | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0019158 | Hepatitis | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0162429 | Malnutrition | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C3642345 | Luminal A Breast Carcinoma | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0205641 | Adenocarcinoma, Basal Cell | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
