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 52426 - 52450 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0023493 Adult T-Cell Lymphoma/Leukemia CNTN2 6900 contactin 2 Q02246
C0023418 leukemia CNTN2 6900 contactin 2 Q02246
C1306459 Primary malignant neoplasm CNTN2 6900 contactin 2 Q02246
C1527336 Sjogren's Syndrome CNTN2 6900 contactin 2 Q02246
C0279592 Adult T Acute Lymphoblastic Leukemia CNTN2 6900 contactin 2 Q02246
C0028945 oligodendroglioma CNTN2 6900 contactin 2 Q02246
C1266184 Atypical Teratoid Rhabdoid Tumor CNTN2 6900 contactin 2 Q02246
C0027651 Neoplasms CNTN2 6900 contactin 2 Q02246
C1510586 Autism Spectrum Disorders CNTN2 6900 contactin 2 Q02246
C0751495 Seizures, Focal CNTN2 6900 contactin 2 Q02246
C4721610 Carcinoma, Ovarian Epithelial CNTN2 6900 contactin 2 Q02246
C0079731 B-Cell Lymphomas CNTN2 6900 contactin 2 Q02246
C0006826 Malignant Neoplasms CNTN2 6900 contactin 2 Q02246
C0162678 Neurofibromatoses CNTN2 6900 contactin 2 Q02246
C0027066 Myoclonus CNTN2 6900 contactin 2 Q02246
C1332986 Childhood Osteosarcoma CNTN2 6900 contactin 2 Q02246
C1140680 Malignant neoplasm of ovary CNTN2 6900 contactin 2 Q02246
C0022408 Arthropathy CNTN2 6900 contactin 2 Q02246
C3714756 Intellectual Disability CNTN2 6900 contactin 2 Q02246
C0149793 Amaurosis Fugax CNTN2 6900 contactin 2 Q02246
C0005956 Bone Marrow Diseases CNTN2 6900 contactin 2 Q02246
C0017638 Glioma CNTN2 6900 contactin 2 Q02246
C0036341 Schizophrenia CNTN2 6900 contactin 2 Q02246
C0029463 Osteosarcoma CNTN2 6900 contactin 2 Q02246
C0699885 Carcinoma of bladder CNTN2 6900 contactin 2 Q02246

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Last updated: August 19, 2024