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
Displaying entries 46226 - 46250 of 62743 in total
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