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:11088
  • asphyxia neonatorum
DOID:9778
  • irritable bowel syndrome
DOID:0110294
  • autosomal recessive limb-girdle muscular dystrophy type 2T
DOID:0111233
  • congenital muscular dystrophy-dystroglycanopathy A14
DOID:0112377
  • muscular dystrophy-dystroglycanopathy type B14
DOID:0112321
  • alacrima, achalasia, and impaired intellectual development syndrome
DOID:0080737
  • Ehlers-Danlos syndrome musculocontractural type 2
DOID:0111277
  • mitochondrial trifunctional protein deficiency
DOID:700
  • mitochondrial metabolism disease
DOID:0070215
  • familial hyperinsulinemic hypoglycemia 4
Displaying entries 1301 - 1310 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