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:397
  • restrictive cardiomyopathy
DOID:0060332
  • mitochondrial complex V (ATP synthase) deficiency nuclear type 3
DOID:0112300
  • spondylometaphyseal dysplasia with cone-rod dystrophy
DOID:0080283
  • developmental and epileptic encephalopathy 55
DOID:0111258
  • pentosuria
DOID:0111756
  • Leber hereditary optic neuropathy with demyelinating disease of CNS
DOID:14701
  • propionic acidemia
DOID:3651
  • pyruvate carboxylase deficiency disease
DOID:0111822
  • CHILD syndrome
DOID:12305
  • Bloch-Sulzberger syndrome
Displaying entries 341 - 350 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