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 60601 - 60625 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0010418 Cryptosporidiosis PTGES3 10728 prostaglandin E synthase 3 Q15185
C1510586 Autism Spectrum Disorders PTGES3 10728 prostaglandin E synthase 3 Q15185
C0029463 Osteosarcoma PTGES3 10728 prostaglandin E synthase 3 Q15185
C0014859 Esophageal Neoplasms PTGES3 10728 prostaglandin E synthase 3 Q15185
C0028064 Niemann-Pick Diseases OGA 10724 O-GlcNAcase O60502
C0030567 Parkinson Disease OGA 10724 O-GlcNAcase O60502
C0039373 Tay-Sachs Disease OGA 10724 O-GlcNAcase O60502
C0011847 Diabetes OGA 10724 O-GlcNAcase O60502
C0087012 Ataxia, Spinocerebellar OGA 10724 O-GlcNAcase O60502
C0011849 Diabetes Mellitus OGA 10724 O-GlcNAcase O60502
C0036161 Sandhoff Disease OGA 10724 O-GlcNAcase O60502
C1565489 Renal Insufficiency OGA 10724 O-GlcNAcase O60502
C0040963 Tricuspid Valve Stenosis OGA 10724 O-GlcNAcase O60502
C0524851 Neurodegenerative Disorders OGA 10724 O-GlcNAcase O60502
C0002395 Alzheimer's Disease OGA 10724 O-GlcNAcase O60502
C0268274 Gangliosidoses, GM2 OGA 10724 O-GlcNAcase O60502
C0020295 Hydronephrosis OGA 10724 O-GlcNAcase O60502
C0242422 Parkinsonian Disorders OGA 10724 O-GlcNAcase O60502
C0021831 Intestinal Diseases OGA 10724 O-GlcNAcase O60502
C0022658 Kidney Diseases OGA 10724 O-GlcNAcase O60502
C0086445 Idiopathic Membranous Glomerulonephritis OGA 10724 O-GlcNAcase O60502
C0085078 Lysosomal Storage Diseases OGA 10724 O-GlcNAcase O60502
C2718068 beta-Galactosidase Deficiency OGA 10724 O-GlcNAcase O60502
C0004153 Atherosclerosis OGA 10724 O-GlcNAcase O60502
C0027651 Neoplasms OGA 10724 O-GlcNAcase O60502

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Last updated: August 19, 2024