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:0090141
  • cortisone reductase deficiency 1
DOID:0110794
  • hereditary spastic paraplegia 42
DOID:8654
  • Hodgkin's lymphoma, mixed cellularity
DOID:9280
  • carbamoyl phosphate synthetase I deficiency disease
DOID:0050648
  • atelosteogenesis
DOID:0111135
  • congenital generalized lipodystrophy type 1
DOID:0111527
  • spinal muscular atrophy with progressive myoclonic epilepsy
DOID:12375
  • bronchopneumonia
DOID:0070261
  • congenital disorder of glycosylation type IIi
DOID:0111458
  • galactose epimerase deficiency
Displaying entries 1611 - 1620 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