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 39826 - 39850 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0028754 Obesity OGA 10724 O-GlcNAcase O60502
C0033788 Pseudo-Hurler Polydystrophy OGA 10724 O-GlcNAcase O60502
C0268731 Renal glomerular disease OGA 10724 O-GlcNAcase O60502
C0010692 Cystitis OGA 10724 O-GlcNAcase O60502
C0178664 Glomerulosclerosis (disorder) OGA 10724 O-GlcNAcase O60502
C0007222 Cardiovascular Diseases OGA 10724 O-GlcNAcase O60502
C0026703 Mucopolysaccharidoses OGA 10724 O-GlcNAcase O60502
C1261473 Sarcoma OGA 10724 O-GlcNAcase O60502
C0006826 Malignant Neoplasms OGA 10724 O-GlcNAcase O60502
C0037899 Sphingolipidoses OGA 10724 O-GlcNAcase O60502
C0752347 Lewy Body Disease OGA 10724 O-GlcNAcase O60502
C0751489 Adult Sandhoff Disease OGA 10724 O-GlcNAcase O60502
C1832916 Timothy syndrome OGA 10724 O-GlcNAcase O60502
C0026697 Mucolipidoses OGA 10724 O-GlcNAcase O60502
C0699790 Colon Carcinoma OGA 10724 O-GlcNAcase O60502
C0038868 Progressive supranuclear palsy OGA 10724 O-GlcNAcase O60502
C0233794 Memory impairment OGA 10724 O-GlcNAcase O60502
C0684249 Carcinoma of lung OGA 10724 O-GlcNAcase O60502
C0027765 nervous system disorder OGA 10724 O-GlcNAcase O60502
C0027051 Myocardial Infarction OGA 10724 O-GlcNAcase O60502
C0009319 Colitis OGA 10724 O-GlcNAcase O60502
C0017205 Gaucher Disease OGA 10724 O-GlcNAcase O60502
C1762616 Meningioma, benign, no ICD-O subtype OGA 10724 O-GlcNAcase O60502
C0011615 Dermatitis, Atopic OGA 10724 O-GlcNAcase O60502
C0041341 Tuberous Sclerosis OGA 10724 O-GlcNAcase O60502

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Last updated: August 19, 2024