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 |
---|---|---|---|---|---|
C0013146 | Drug abuse | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0341858 | Endometriosis of uterus | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0002395 | Alzheimer's Disease | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0010068 | Coronary heart disease | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0033578 | Prostatic Neoplasms | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0020302 | Hydrophthalmos | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0008370 | Cholestasis | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0023452 | Childhood Acute Lymphoblastic Leukemia | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0265219 | Miller Dieker syndrome | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0023903 | Liver neoplasms | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0004698 | Balkan Nephropathy | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0152013 | Adenocarcinoma of lung (disorder) | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0031269 | Peutz-Jeghers Syndrome | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C1857276 | Trichohepatoenteric Syndrome | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0686347 | Tardive Dyskinesia | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0011847 | Diabetes | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0524851 | Neurodegenerative Disorders | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0948008 | Ischemic stroke | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0241910 | Autoimmune Chronic Hepatitis | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C1858142 | ICHTHYOSIS, LAMELLAR, 3 | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0013336 | Dwarfism | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0017605 | Angle Closure Glaucoma | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0563625 | Agnosia for Pain | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C1291245 | Cortisone reductase deficiency | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C2919945 | Cavernous Hemangioma of Brain | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
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Last updated: August 19, 2024