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 February 28, 2024
DisGeNET February 14, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Disease ID ▲ Disease Name Gene Symbol Gene ID
  • dominant optic atrophy plus syndrome
  • lateral meningocele syndrome
  • D-2-hydroxyglutaric aciduria 2
  • large congenital melanocytic nevus
  • inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1
  • mucopolysaccharidosis Ih/s
  • mucopolysaccharidosis Ih
  • mucopolysaccharidosis IVA
  • mucopolysaccharidosis type IVB
  • mucopolysaccharidosis type IIIC
Displaying entries 761 - 770 of 1885 in total

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