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 42651 - 42675 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C0007137 Squamous cell carcinoma ENO1 2023 enolase 1 P06733
C0949690 Spondylarthritis ENO1 2023 enolase 1 P06733
C0027051 Myocardial Infarction ENO1 2023 enolase 1 P06733
C0004096 Asthma ENO1 2023 enolase 1 P06733
C0008354 Cholera ENO1 2023 enolase 1 P06733
C2609129 Autoimmune pancreatitis ENO1 2023 enolase 1 P06733
C0026850 Muscular Dystrophy ENO1 2023 enolase 1 P06733
C0206698 Cholangiocarcinoma ENO1 2023 enolase 1 P06733
C0021400 Influenza ENO1 2023 enolase 1 P06733
C0022578 Keratoconus ENO1 2023 enolase 1 P06733
C0494463 Alzheimer Disease, Late Onset ENO1 2023 enolase 1 P06733
C0345904 Malignant neoplasm of liver ENO1 2023 enolase 1 P06733
C1561643 Chronic Kidney Diseases ENO1 2023 enolase 1 P06733
C0011265 Presenile dementia ENO1 2023 enolase 1 P06733
C0019112 Hemorrhoids ENO1 2023 enolase 1 P06733
C0016053 Fibromyalgia ENO1 2023 enolase 1 P06733
C0003469 Anxiety Disorders ENO1 2023 enolase 1 P06733
C0205645 Adenocarcinoma, Tubular ENO1 2023 enolase 1 P06733
C1852467 Creutzfeldt-Jakob Disease, Sporadic ENO1 2023 enolase 1 P06733
C0011849 Diabetes Mellitus ENO1 2023 enolase 1 P06733
C0162565 Acute intermittent porphyria ENO1 2023 enolase 1 P06733
C1851841 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 1 ENO1 2023 enolase 1 P06733
C0205698 Undifferentiated carcinoma ENO1 2023 enolase 1 P06733
C0021390 Inflammatory Bowel Diseases ENO1 2023 enolase 1 P06733
C0014859 Esophageal Neoplasms ENO1 2023 enolase 1 P06733

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Last updated: August 19, 2024