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:0060280
  • primary pigmented nodular adrenocortical disease
DOID:0060283
  • peeling skin syndrome
DOID:0060284
  • paroxysmal nocturnal hemoglobinuria
DOID:0060292
  • X-linked chondrodysplasia punctata 1
DOID:0060307
  • autosomal dominant intellectual developmental disorder
DOID:0060309
  • syndromic X-linked intellectual disability
DOID:0060318
  • acute promyelocytic leukemia
DOID:0060332
  • mitochondrial complex V (ATP synthase) deficiency nuclear type 3
DOID:0060335
  • autosomal dominant sideroblastic anemia 4
DOID:0060350
  • adenine phosphoribosyltransferase deficiency
Displaying entries 181 - 190 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