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:0112237
  • lissencephaly 1
DOID:0060469
  • Miller-Dieker lissencephaly syndrome
DOID:318
  • progressive muscular atrophy
DOID:0110530
  • autosomal recessive nonsyndromic deafness 84B
DOID:0110474
  • autosomal recessive nonsyndromic deafness 18B
DOID:0110480
  • autosomal recessive nonsyndromic deafness 22
DOID:0080319
  • X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia
DOID:0111839
  • congenital disorder of glycosylation Icc
DOID:0081183
  • autosomal recessive intellectual developmental disorder 7
DOID:612
  • primary immunodeficiency disease
Displaying entries 391 - 400 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