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 40876 - 40900 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C0017168 Gastroesophageal reflux disease FCSK 197258 fucose kinase Q8N0W3
C0029124 Optic Atrophy FCSK 197258 fucose kinase Q8N0W3
C0085207 Gestational Diabetes FCN3 8547 ficolin 3 O75636
C0024143 Lupus Nephritis FCN3 8547 ficolin 3 O75636
C1140680 Malignant neoplasm of ovary FCN3 8547 ficolin 3 O75636
C0003257 Antibody Deficiency Syndrome FCN3 8547 ficolin 3 O75636
C0006826 Malignant Neoplasms FCN3 8547 ficolin 3 O75636
C0023343 Leprosy FCN3 8547 ficolin 3 O75636
C0011860 Diabetes Mellitus, Non-Insulin-Dependent FCN3 8547 ficolin 3 O75636
C0027051 Myocardial Infarction FCN3 8547 ficolin 3 O75636
C0162871 Aortic Aneurysm, Abdominal FCN3 8547 ficolin 3 O75636
C0024141 Lupus Erythematosus, Systemic FCN3 8547 ficolin 3 O75636
C2239176 Liver carcinoma FCN3 8547 ficolin 3 O75636
C3665596 Warts FCN3 8547 ficolin 3 O75636
C0010346 Crohn Disease FCN3 8547 ficolin 3 O75636
C0206062 Lung Diseases, Interstitial FCN3 8547 ficolin 3 O75636
C0010068 Coronary heart disease FCN3 8547 ficolin 3 O75636
C0020538 Hypertensive disease FCN3 8547 ficolin 3 O75636
C0041296 Tuberculosis FCN3 8547 ficolin 3 O75636
C0043037 Common wart FCN3 8547 ficolin 3 O75636
C0919267 ovarian neoplasm FCN3 8547 ficolin 3 O75636
C0036421 Systemic Scleroderma FCN3 8547 ficolin 3 O75636
C4721610 Carcinoma, Ovarian Epithelial FCN3 8547 ficolin 3 O75636
C0002736 Amyotrophic Lateral Sclerosis FCN3 8547 ficolin 3 O75636
C0085580 Essential Hypertension FCN3 8547 ficolin 3 O75636

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Last updated: August 19, 2024