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:0111067
  • congenital bile acid synthesis defect 6
DOID:0060307
  • autosomal dominant intellectual developmental disorder
DOID:0081215
  • autosomal recessive intellectual developmental disorder 52
DOID:0050645
  • arterial tortuosity syndrome
DOID:0111071
  • congenital bile acid synthesis defect 1
DOID:0112160
  • autosomal dominant nonsyndromic deafness 79
DOID:0110352
  • retinitis pigmentosa 59
DOID:0080473
  • developmental delay and seizures with or without movement abnormalities
DOID:0050807
  • Kahrizi syndrome
DOID:0080568
  • congenital disorder of glycosylation Iq
Displaying entries 121 - 130 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