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
DOID:0080101
  • Compton-North congenital myopathy
DOID:0050523
  • adult T-cell leukemia/lymphoma
DOID:0111691
  • familial adult myoclonic epilepsy 5
DOID:0070259
  • congenital disorder of glycosylation type IIg
DOID:0070269
  • congenital disorder of glycosylation type IIq
DOID:0070262
  • congenital disorder of glycosylation type IIj
DOID:0111673
  • Saul-Wilson syndrome
DOID:0070261
  • congenital disorder of glycosylation type IIi
DOID:0070264
  • congenital disorder of glycosylation type IIl
DOID:0070257
  • congenital disorder of glycosylation type IIe
Displaying entries 691 - 700 of 1885 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 v3.5.0
  • Last updated: March 25, 2024