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 1801 - 1825 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C1879321 Acute Myeloid Leukemia (AML-M2) AGRN 375790 agrin O00468
C0020224 Polyhydramnios AGRN 375790 agrin O00468
C0575158 Kyphoscoliosis deformity of spine AGRN 375790 agrin O00468
C0751401 Ophthalmoparesis AGRN 375790 agrin O00468
C0005745 Blepharoptosis AGRN 375790 agrin O00468
C0015469 Facial paralysis AGRN 375790 agrin O00468
C0026691 Mucocutaneous Lymph Node Syndrome FCN1 2219 ficolin 1 O00602
C0027051 Myocardial Infarction FCN1 2219 ficolin 1 O00602
C0015674 Chronic Fatigue Syndrome FCN1 2219 ficolin 1 O00602
C0027651 Neoplasms FCN1 2219 ficolin 1 O00602
C0006826 Malignant Neoplasms FCN1 2219 ficolin 1 O00602
C0917805 Transient Cerebral Ischemia FCN1 2219 ficolin 1 O00602
C0003873 Rheumatoid Arthritis FCN1 2219 ficolin 1 O00602
C0023348 Leprosy, Lepromatous FCN1 2219 ficolin 1 O00602
C0020473 Hyperlipidemia FCN1 2219 ficolin 1 O00602
C0010674 Cystic Fibrosis FCN1 2219 ficolin 1 O00602
C1306459 Primary malignant neoplasm FCN1 2219 ficolin 1 O00602
C0023343 Leprosy FCN1 2219 ficolin 1 O00602
C0007785 Cerebral Infarction FCN1 2219 ficolin 1 O00602
C0004364 Autoimmune Diseases FCN1 2219 ficolin 1 O00602
C0024143 Lupus Nephritis FCN1 2219 ficolin 1 O00602
C0003864 Arthritis FCN1 2219 ficolin 1 O00602
C0009402 Colorectal Carcinoma FCN1 2219 ficolin 1 O00602
C0007786 Brain Ischemia FCN1 2219 ficolin 1 O00602
C0035436 Rheumatic Fever FCN1 2219 ficolin 1 O00602

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Last updated: August 19, 2024