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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol ▼ | Gene ID | Gene Name | UniProt ID |
---|---|---|---|---|---|
C0025517 | Metabolic Diseases | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0007682 | CNS disorder | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0008677 | Bronchitis, Chronic | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0024623 | Malignant neoplasm of stomach | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C2711227 | Steatohepatitis | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0022104 | Irritable Bowel Syndrome | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0030297 | Pancreatic Neoplasm | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C3463824 | MYELODYSPLASTIC SYNDROME | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0346647 | Malignant neoplasm of pancreas | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0278510 | Childhood Medulloblastoma | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0003125 | Anorexia Nervosa | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0003467 | Anxiety | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0034067 | Pulmonary Emphysema | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0020676 | Hypothyroidism | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0585442 | Osteosarcoma of bone | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0342474 | Lipoid congenital adrenal hyperplasia | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0752347 | Lewy Body Disease | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0027947 | Neutropenia | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0017606 | Primary angle-closure glaucoma | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0919267 | ovarian neoplasm | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0020598 | Hypocalcemia | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0029124 | Optic Atrophy | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0085584 | Encephalopathies | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0265224 | Freeman-Sheldon syndrome | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0699791 | Stomach Carcinoma | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
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Last updated: August 19, 2024