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
  • Stiff-Person syndrome
  • autosomal recessive nonsyndromic deafness 22
  • autosomal recessive limb-girdle muscular dystrophy type 2M
  • wrinkly skin syndrome
  • pulmonary emphysema
  • syndromic X-linked intellectual disability Hedera type
  • phosphoglycerate kinase 1 deficiency
  • congenital nonspherocytic hemolytic anemia
  • cortisone reductase deficiency
  • Ehlers-Danlos syndrome musculocontractural type 2
Displaying entries 31 - 40 of 1611 in total

International Collaboration

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


Supported by JST NBDC Grant Number JPMJND2204

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