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:0110279
  • autosomal recessive limb-girdle muscular dystrophy type 2E
DOID:0110282
  • autosomal recessive limb-girdle muscular dystrophy type 2H
DOID:0060255
  • rippling muscle disease 2
DOID:0080094
  • myofibrillar myopathy 3
DOID:0110277
  • autosomal recessive limb-girdle muscular dystrophy type 2C
DOID:0110273
  • autosomal dominant limb-girdle muscular dystrophy
DOID:0111671
  • primary hyperoxaluria type 2
DOID:0070259
  • congenital disorder of glycosylation type IIg
DOID:0070382
  • developmental and epileptic encephalopathy 95
DOID:5804
  • discrete subaortic stenosis
Displaying entries 1861 - 1870 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