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 39801 - 39825 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C1848922 Hexosaminidase alpha-Subunit Deficiency (Variant B) OGA 10724 O-GlcNAcase O60502
C0036572 Seizures OGA 10724 O-GlcNAcase O60502
C0030319 Panic Disorder OGA 10724 O-GlcNAcase O60502
C4721610 Carcinoma, Ovarian Epithelial OGA 10724 O-GlcNAcase O60502
C2239176 Liver carcinoma OGA 10724 O-GlcNAcase O60502
C1704321 Nephrotic Syndrome, Minimal Change OGA 10724 O-GlcNAcase O60502
C0949664 Tauopathies OGA 10724 O-GlcNAcase O60502
C0085207 Gestational Diabetes OGA 10724 O-GlcNAcase O60502
C0017083 Gangliosidoses OGA 10724 O-GlcNAcase O60502
C0025286 Meningioma OGA 10724 O-GlcNAcase O60502
C0271650 Impaired glucose tolerance OGA 10724 O-GlcNAcase O60502
C0037579 Soft Tissue Neoplasms OGA 10724 O-GlcNAcase O60502
C0009375 Colonic Neoplasms OGA 10724 O-GlcNAcase O60502
C4551686 Malignant neoplasm of soft tissue OGA 10724 O-GlcNAcase O60502
C0014038 Encephalitis OGA 10724 O-GlcNAcase O60502
C0014544 Epilepsy OGA 10724 O-GlcNAcase O60502
C0524620 Metabolic Syndrome X OGA 10724 O-GlcNAcase O60502
C0002736 Amyotrophic Lateral Sclerosis OGA 10724 O-GlcNAcase O60502
C0023890 Liver Cirrhosis OGA 10724 O-GlcNAcase O60502
C0751491 Juvenile Sandhoff Disease OGA 10724 O-GlcNAcase O60502
C0026764 Multiple Myeloma OGA 10724 O-GlcNAcase O60502
C0018801 Heart failure OGA 10724 O-GlcNAcase O60502
C0017636 Glioblastoma OGA 10724 O-GlcNAcase O60502
C0162429 Malnutrition OGA 10724 O-GlcNAcase O60502
C0020725 Type II Mucolipidosis OGA 10724 O-GlcNAcase O60502

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Last updated: August 19, 2024