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 12826 - 12850 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0019569 Hirschsprung Disease ENO2 2026 enolase 2 P09104
C0206686 Adrenocortical carcinoma ENO2 2026 enolase 2 P09104
C1332977 Childhood Leukemia ENO2 2026 enolase 2 P09104
C4048158 Convulsions ENO2 2026 enolase 2 P09104
C0011854 Diabetes Mellitus, Insulin-Dependent ENO2 2026 enolase 2 P09104
C0020433 Hyperbilirubinemia ENO2 2026 enolase 2 P09104
C0041327 Tuberculosis, Pulmonary ENO2 2026 enolase 2 P09104
C0242422 Parkinsonian Disorders ENO2 2026 enolase 2 P09104
C0004045 Asphyxia Neonatorum ENO2 2026 enolase 2 P09104
C0152021 Congenital heart disease ENO2 2026 enolase 2 P09104
C0033845 Pseudotumor Cerebri ENO2 2026 enolase 2 P09104
C0031117 Peripheral Neuropathy ENO2 2026 enolase 2 P09104
C0040517 Gilles de la Tourette syndrome ENO2 2026 enolase 2 P09104
C0270824 Visual seizure ENO2 2026 enolase 2 P09104
C0041296 Tuberculosis ENO2 2026 enolase 2 P09104
C0041696 Unipolar Depression ENO2 2026 enolase 2 P09104
C0035412 Rhabdomyosarcoma ENO2 2026 enolase 2 P09104
C0006118 Brain Neoplasms ENO2 2026 enolase 2 P09104
C0007133 Carcinoma, Papillary ENO2 2026 enolase 2 P09104
C0020615 Hypoglycemia ENO2 2026 enolase 2 P09104
C0268398 Familial lichen amyloidosis ENO2 2026 enolase 2 P09104
C0028945 oligodendroglioma ENO2 2026 enolase 2 P09104
C0034050 Pulmonary Alveolar Proteinosis ENO2 2026 enolase 2 P09104
C0018802 Congestive heart failure ENO2 2026 enolase 2 P09104
C0025309 Meningoencephalitis ENO2 2026 enolase 2 P09104

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Last updated: August 19, 2024