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 10726 - 10750 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C0008487 Chordoma ACAN 176 aggrecan P16112
C0004352 Autistic Disorder ACAN 176 aggrecan P16112
C1260873 Aortic valve disorder ACAN 176 aggrecan P16112
C0149630 Bicuspid aortic valve ACAN 176 aggrecan P16112
C0030481 Tropical Spastic Paraparesis ACAN 176 aggrecan P16112
C1692886 Arthritis, Bacterial ACAN 176 aggrecan P16112
C0004681 Bagassosis ACAN 176 aggrecan P16112
C0003869 Arthritis, Infectious ACAN 176 aggrecan P16112
C0085700 Chondromalacia ACAN 176 aggrecan P16112
C0037369 Smoking ACAN 176 aggrecan P16112
C3808739 MYASTHENIC SYNDROME, CONGENITAL, 8 AGRN 375790 agrin O00468
C0023467 Leukemia, Myelocytic, Acute AGRN 375790 agrin O00468
C0152013 Adenocarcinoma of lung (disorder) AGRN 375790 agrin O00468
C0028738 Nystagmus AGRN 375790 agrin O00468
C0238463 Papillary thyroid carcinoma AGRN 375790 agrin O00468
C0036572 Seizures AGRN 375790 agrin O00468
C0018784 Sensorineural Hearing Loss (disorder) AGRN 375790 agrin O00468
C0751883 Congenital Myasthenic Syndromes, Postsynaptic AGRN 375790 agrin O00468
C0751882 Myasthenic Syndromes, Congenital AGRN 375790 agrin O00468
C0002395 Alzheimer's Disease AGRN 375790 agrin O00468
C0026998 Acute Myeloid Leukemia, M1 AGRN 375790 agrin O00468
C0014877 Esotropia AGRN 375790 agrin O00468
C1306459 Primary malignant neoplasm AGRN 375790 agrin O00468
C0520680 Sleep Apnea, Central AGRN 375790 agrin O00468
C0017168 Gastroesophageal reflux disease AGRN 375790 agrin O00468

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Last updated: August 19, 2024