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 351 - 375 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0027651 Neoplasms SDC3 9672 syndecan 3 O75056
C0276496 Familial Alzheimer Disease (FAD) SDC3 9672 syndecan 3 O75056
C0235974 Pancreatic carcinoma SDC3 9672 syndecan 3 O75056
C1306459 Primary malignant neoplasm SDC3 9672 syndecan 3 O75056
C0524620 Metabolic Syndrome X SDC3 9672 syndecan 3 O75056
C0003873 Rheumatoid Arthritis SDC3 9672 syndecan 3 O75056
C0002395 Alzheimer's Disease SDC3 9672 syndecan 3 O75056
C0019196 Hepatitis C SDC3 9672 syndecan 3 O75056
C1857276 Trichohepatoenteric Syndrome LPIN2 9663 lipin 2 Q92539
C0002876 Congenital dyserythropoietic anemia LPIN2 9663 lipin 2 Q92539
C0011860 Diabetes Mellitus, Non-Insulin-Dependent LPIN2 9663 lipin 2 Q92539
C0011849 Diabetes Mellitus LPIN2 9663 lipin 2 Q92539
C1834531 MYOPIA 2 (disorder) LPIN2 9663 lipin 2 Q92539
C0011847 Diabetes LPIN2 9663 lipin 2 Q92539
C0002871 Anemia LPIN2 9663 lipin 2 Q92539
C0010346 Crohn Disease LPIN2 9663 lipin 2 Q92539
C0035021 Relapsing Fever LPIN2 9663 lipin 2 Q92539
C0039103 Synovitis LPIN2 9663 lipin 2 Q92539
C0028754 Obesity LPIN2 9663 lipin 2 Q92539
C0027092 Myopia LPIN2 9663 lipin 2 Q92539
C0023530 Leukopenia LPIN2 9663 lipin 2 Q92539
C0025517 Metabolic Diseases LPIN2 9663 lipin 2 Q92539
C0003873 Rheumatoid Arthritis LPIN2 9663 lipin 2 Q92539
C0949116 Congenital hypoplastic anemia LPIN2 9663 lipin 2 Q92539
C3714772 Recurrent fevers LPIN2 9663 lipin 2 Q92539

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Last updated: August 19, 2024