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
  • congenital stationary night blindness
  • Charcot-Marie-Tooth disease type 2
  • visceral heterotaxy
  • congenital adrenal insufficiency
  • hereditary sensory neuropathy
  • congenital muscular dystrophy
  • Fukuyama congenital muscular dystrophy
  • Walker-Warburg syndrome
  • Lennox-Gastaut syndrome
  • West syndrome
Displaying entries 31 - 40 of 1675 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