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 12801 - 12825 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0524620 Metabolic Syndrome X ENO2 2026 enolase 2 P09104
C0017925 Glycogen Storage Disease Type VI ENO2 2026 enolase 2 P09104
C0024115 Lung diseases ENO2 2026 enolase 2 P09104
C1306459 Primary malignant neoplasm ENO2 2026 enolase 2 P09104
C0027665 Neoplasms, Nerve Tissue ENO2 2026 enolase 2 P09104
C0751495 Seizures, Focal ENO2 2026 enolase 2 P09104
C0023452 Childhood Acute Lymphoblastic Leukemia ENO2 2026 enolase 2 P09104
C0007134 Renal Cell Carcinoma ENO2 2026 enolase 2 P09104
C1852467 Creutzfeldt-Jakob Disease, Sporadic ENO2 2026 enolase 2 P09104
C0079744 Diffuse Large B-Cell Lymphoma ENO2 2026 enolase 2 P09104
C1879321 Acute Myeloid Leukemia (AML-M2) ENO2 2026 enolase 2 P09104
C0751688 Malignant Squamous Cell Neoplasm ENO2 2026 enolase 2 P09104
C0524851 Neurodegenerative Disorders ENO2 2026 enolase 2 P09104
C0029124 Optic Atrophy ENO2 2026 enolase 2 P09104
C0339527 Leber Congenital Amaurosis ENO2 2026 enolase 2 P09104
C0001430 Adenoma ENO2 2026 enolase 2 P09104
C0010308 Congenital Hypothyroidism ENO2 2026 enolase 2 P09104
C1862382 SVEINSSON CHORIORETINAL ATROPHY ENO2 2026 enolase 2 P09104
C0600327 Toxic Shock Syndrome ENO2 2026 enolase 2 P09104
C0015397 Disorder of eye ENO2 2026 enolase 2 P09104
C0751956 Acute Cerebrovascular Accidents ENO2 2026 enolase 2 P09104
C1851585 MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA ENO2 2026 enolase 2 P09104
C0005695 Bladder Neoplasm ENO2 2026 enolase 2 P09104
C4721453 Peripheral Nervous System Diseases ENO2 2026 enolase 2 P09104
C3550973 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5 ENO2 2026 enolase 2 P09104

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Last updated: August 19, 2024