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 59776 - 59800 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0025202 melanoma IL1RAPL1 11141 interleukin 1 receptor accessory protein like 1 Q9NZN1
C0494475 Tonic - clonic seizures IL1RAPL1 11141 interleukin 1 receptor accessory protein like 1 Q9NZN1
C0342482 X-linked Adrenal Hypoplasia IL1RAPL1 11141 interleukin 1 receptor accessory protein like 1 Q9NZN1
C1458155 Mammary Neoplasms IL1RAPL1 11141 interleukin 1 receptor accessory protein like 1 Q9NZN1
C0795887 Complex Glycerol Kinase Deficiency IL1RAPL1 11141 interleukin 1 receptor accessory protein like 1 Q9NZN1
C0079744 Diffuse Large B-Cell Lymphoma IL1RAPL1 11141 interleukin 1 receptor accessory protein like 1 Q9NZN1
C1269683 Major Depressive Disorder HACD3 51495 3-hydroxyacyl-CoA dehydratase 3 Q9P035
C0011581 Depressive disorder HACD3 51495 3-hydroxyacyl-CoA dehydratase 3 Q9P035
C0011570 Mental Depression HACD3 51495 3-hydroxyacyl-CoA dehydratase 3 Q9P035
C0004096 Asthma ORMDL1 94101 ORMDL sphingolipid biosynthesis regulator 1 Q9P0S3
C0036341 Schizophrenia NTM 50863 neurotrimin Q9P121
C0007766 Intracranial Aneurysm NTM 50863 neurotrimin Q9P121
C0027651 Neoplasms NTM 50863 neurotrimin Q9P121
C1306459 Primary malignant neoplasm NTM 50863 neurotrimin Q9P121
C0041327 Tuberculosis, Pulmonary NTM 50863 neurotrimin Q9P121
C0041296 Tuberculosis NTM 50863 neurotrimin Q9P121
C0018801 Heart failure NTM 50863 neurotrimin Q9P121
C1269683 Major Depressive Disorder NTM 50863 neurotrimin Q9P121
C3160718 PARKINSON DISEASE, LATE-ONSET NTM 50863 neurotrimin Q9P121
C0006826 Malignant Neoplasms NTM 50863 neurotrimin Q9P121
C0027051 Myocardial Infarction NTM 50863 neurotrimin Q9P121
C0026916 Mycobacterium avium-intracellulare Infection NTM 50863 neurotrimin Q9P121
C0238462 Medullary carcinoma of thyroid NTM 50863 neurotrimin Q9P121
C1853230 Aphakia, congenital primary NTM 50863 neurotrimin Q9P121
C0017168 Gastroesophageal reflux disease NTM 50863 neurotrimin Q9P121

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Last updated: August 19, 2024