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:0080257
  • autosomal recessive congenital ichthyosis 13
DOID:0080250
  • erythrokeratodermia variabilis et progressiva 4
DOID:0080246
  • Galloway-Mowat syndrome 4
DOID:0080240
  • non-syndromic X-linked intellectual disability 106
DOID:0080235
  • autosomal dominant intellectual developmental disorder 48
DOID:0080219
  • dystransthyretinemic hyperthyroxinemia
DOID:0080217
  • lysosomal acid lipase deficiency
DOID:0080208
  • metabolic dysfunction-associated steatotic liver disease
DOID:0080205
  • CAKUT
DOID:0080201
  • Peters plus syndrome
Displaying entries 1501 - 1510 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