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:0080139
  • multiple congenital anomalies-hypotonia-seizures syndrome 2
DOID:0080140
  • multiple congenital anomalies-hypotonia-seizures syndrome 3
DOID:0080143
  • congenital fibrosis of the extraocular muscles
DOID:0080144
  • childhood acute lymphocytic leukemia
DOID:0080147
  • lymphoblastic lymphoma
DOID:0080153
  • medium chain acyl-CoA dehydrogenase deficiency
DOID:0080154
  • short chain acyl-CoA dehydrogenase deficiency
DOID:0080155
  • very long chain acyl-CoA dehydrogenase deficiency
DOID:0080159
  • Cryptococcal meningitis
DOID:0080162
  • lupus nephritis
Displaying entries 361 - 370 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

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  • Last updated: March 25, 2024