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 47576 - 47600 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
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
C0442874 Neuropathy ENO2 2026 enolase 2 P09104
C0019337 Heroin Dependence ENO2 2026 enolase 2 P09104
C0027651 Neoplasms STS 412 steroid sulfatase P08842
C2720163 Placental Steroid Sulfatase Deficiency STS 412 steroid sulfatase P08842
C0162809 Kallmann Syndrome STS 412 steroid sulfatase P08842
C0079588 Ichthyosis, X-Linked STS 412 steroid sulfatase P08842
C0025202 melanoma STS 412 steroid sulfatase P08842
C0476089 Endometrial Carcinoma STS 412 steroid sulfatase P08842

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Last updated: August 19, 2024