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:0070243
  • primary coenzyme Q10 deficiency 6
DOID:0060335
  • autosomal dominant sideroblastic anemia 4
DOID:0111131
  • focal segmental glomerulosclerosis 6
DOID:0111974
  • immunodeficiency 59
DOID:2580
  • rhizomelic chondrodysplasia punctata
DOID:0110853
  • rhizomelic chondrodysplasia punctata type 3
DOID:0112349
  • hereditary spastic paraplegia 81
DOID:0080257
  • autosomal recessive congenital ichthyosis 13
DOID:0060098
  • osteoblastoma
DOID:0060357
  • chylomicron retention disease
Displaying entries 1811 - 1820 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