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 43226 - 43250 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0220981 Metabolic acidosis OGDH 4967 oxoglutarate dehydrogenase Q02218
C0018801 Heart failure OGDH 4967 oxoglutarate dehydrogenase Q02218
C0006826 Malignant Neoplasms OGDH 4967 oxoglutarate dehydrogenase Q02218
C0751435 Hyperphenylalaninaemia OGDH 4967 oxoglutarate dehydrogenase Q02218
C0030481 Tropical Spastic Paraparesis CNTN2 6900 contactin 2 Q02246
C0234533 Generalized seizures CNTN2 6900 contactin 2 Q02246
C0002395 Alzheimer's Disease CNTN2 6900 contactin 2 Q02246
C0004364 Autoimmune Diseases CNTN2 6900 contactin 2 Q02246
C0023492 Leukemia, T-Cell CNTN2 6900 contactin 2 Q02246
C0005684 Malignant neoplasm of urinary bladder CNTN2 6900 contactin 2 Q02246
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

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Last updated: August 19, 2024