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 46176 - 46200 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C0036631 Seminoma CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813
C0025202 melanoma CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813
C0524662 Opiate Addiction CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813
C0033860 Psoriasis CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813
C0011581 Depressive disorder CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813
C0003469 Anxiety Disorders CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813
C0025149 Medulloblastoma CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813
C1568868 Oral Mucositis CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813
C4721610 Carcinoma, Ovarian Epithelial CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813
C0009402 Colorectal Carcinoma CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813
C0002874 Aplastic Anemia CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813
C0026764 Multiple Myeloma CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813
C0206686 Adrenocortical carcinoma CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813
C1704272 Benign Prostatic Hyperplasia CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813
C0268285 Adrenal hyperplasia, congenital, type 5 CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813
C0476089 Endometrial Carcinoma CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813
C0036341 Schizophrenia CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813
C0400966 Non-alcoholic Fatty Liver Disease CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813
C1332206 Adult Lymphoma CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813
C0018802 Congestive heart failure CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813
C0004779 Basal Cell Nevus Syndrome CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813
C0751956 Acute Cerebrovascular Accidents CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813
C1332977 Childhood Leukemia CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813
C0017636 Glioblastoma CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813
C0023487 Acute Promyelocytic Leukemia CYP2B6 1555 cytochrome P450 family 2 subfamily B member 6 P20813

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Last updated: August 19, 2024