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 42951 - 42975 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
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
C0524620 Metabolic Syndrome X CNTN2 6900 contactin 2 Q02246
C0017636 Glioblastoma CNTN2 6900 contactin 2 Q02246
C0037928 Spinal Cord Diseases CNTN2 6900 contactin 2 Q02246
C0024299 Lymphoma CNTN2 6900 contactin 2 Q02246
C0242287 Isaacs syndrome CNTN2 6900 contactin 2 Q02246
C0555198 Malignant Glioma CNTN2 6900 contactin 2 Q02246
C0036572 Seizures CNTN2 6900 contactin 2 Q02246
C0030567 Parkinson Disease CNTN2 6900 contactin 2 Q02246
C0280475 Childhood Oligodendroglioma CNTN2 6900 contactin 2 Q02246
C0024314 Lymphoproliferative Disorders CNTN2 6900 contactin 2 Q02246
C0003864 Arthritis CNTN2 6900 contactin 2 Q02246

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Last updated: August 19, 2024