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:0080154
  • short chain acyl-CoA dehydrogenase deficiency
DOID:8791
  • breast carcinoma in situ
DOID:0111522
  • autosomal recessive progressive external ophthalmoplegia 1
DOID:0111276
  • sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
DOID:0080122
  • Alpers-Huttenlocher syndrome
DOID:0080123
  • mitochondrial DNA depletion syndrome 4b
DOID:0111521
  • autosomal dominant progressive external ophthalmoplegia 1
DOID:12558
  • chronic progressive external ophthalmoplegia
DOID:574
  • peripheral nervous system disease
DOID:3911
  • progeria
Displaying entries 471 - 480 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