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 43251 - 43275 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
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
C0005695 Bladder Neoplasm CNTN2 6900 contactin 2 Q02246
C0919267 ovarian neoplasm CNTN2 6900 contactin 2 Q02246
C1332977 Childhood Leukemia CNTN2 6900 contactin 2 Q02246
C1332206 Adult Lymphoma CNTN2 6900 contactin 2 Q02246
C0003873 Rheumatoid Arthritis CNTN2 6900 contactin 2 Q02246
C0004238 Atrial Fibrillation CNTN2 6900 contactin 2 Q02246
C0751396 Well Differentiated Oligodendroglioma CNTN2 6900 contactin 2 Q02246
C0175697 Van der Woude syndrome CNTN2 6900 contactin 2 Q02246
C0393819 Polyradiculoneuropathy, Chronic Inflammatory Demyelinating CNTN2 6900 contactin 2 Q02246
C0585442 Osteosarcoma of bone CNTN2 6900 contactin 2 Q02246
C0024054 Lown-Ganong-Levine Syndrome CNTN2 6900 contactin 2 Q02246
C0025958 Microcephaly CNTN2 6900 contactin 2 Q02246
C0267026 Actinic cheilitis CNTN2 6900 contactin 2 Q02246
C1621958 Glioblastoma Multiforme CNTN2 6900 contactin 2 Q02246
C0524851 Neurodegenerative Disorders CNTN2 6900 contactin 2 Q02246

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Last updated: August 19, 2024