GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Database Last Updated
Alliance of Genome Resources October 28, 2022
DisGeNET June 29,2021
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Disease ID Disease Name Gene Symbol Gene ID ▲
DOID:0080388
  • nephrotic syndrome type 7
DOID:0050561
  • Lennox-Gastaut syndrome
DOID:384
  • Wolff-Parkinson-White syndrome
DOID:0110312
  • hypertrophic cardiomyopathy 6
DOID:0090101
  • lethal congenital glycogen storage disease of heart
DOID:0070243
  • primary coenzyme Q10 deficiency 6
DOID:3204
  • neurilemmomatosis
DOID:0060335
  • autosomal dominant sideroblastic anemia 4
DOID:0111131
  • focal segmental glomerulosclerosis 6
DOID:0111974
  • immunodeficiency 59
Displaying entries 1601 - 1610 of 1675 in total
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International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

  • © GlyCosmos Portal v3.2.1
  • Last updated: April 24, 2023