Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
Resources Genes Glycoproteins Lectins Glycolipids Glycans Pathways Diseases Organisms
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Other Information
Release Statistics Download
Tools
SugarDrawer GlycanBuilder Glycan Converters GlycoMaple GlycomeAtlas LM-GlycomeAtlas GALAXY MCAW GlycoSim GRable
Search Tools
Cross Search Glycan Search Publication Search Programmatic Access
Standards Ontologies Notations
GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 4326 - 4350 of 4649 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:0060020
  • reticular dysgenesis
  • Aliases:
    • De Vaal disease
Homo sapiens (human)
DOID:0060019
  • coronin-1A deficiency
Homo sapiens (human)
DOID:0060013
  • X-linked severe combined immunodeficiency
  • Aliases:
    • SCID-X1
    • XSCID
    • gamma chain deficiency
    • thymic epithelial hypoplasia
Homo sapiens (human)
DOID:0060010
  • Omenn syndrome
  • Aliases:
    • combined immunodeficiency with hypereosinophilia
Homo sapiens (human)
DOID:0060009
  • MHC class I deficiency
  • Aliases:
    • BLS, TYPE I
    • BLSI
    • HLA CLASS I DEFICIENCY
    • bare lymphocyte syndrome type I
Homo sapiens (human)
DOID:0060001
  • withdrawal disorder
Homo sapiens (human)
DOID:0060000
  • infective endocarditis
Homo sapiens (human)
DOID:0050998
  • nonprogressive cerebellar ataxia with mental retardation
Homo sapiens (human)
DOID:0050997
  • cerebellar ataxia, mental retardation and dysequlibrium syndrome
  • Aliases:
    • CAMRQ
    • Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome 1 (CAMRQ1)
    • Uner Tan syndrome
    • VLDLR Cerebellar Hypoplasia
Homo sapiens (human)
DOID:0050994
  • episodic ataxia type 6
Homo sapiens (human)
DOID:0050990
  • episodic ataxia type 2
Homo sapiens (human)
DOID:0050989
  • episodic ataxia type 1
Homo sapiens (human)
DOID:0050987
  • hypomyelinating leukoencephalopathy
Homo sapiens (human)
DOID:0050986
  • spinocerebellar ataxia type 40
Homo sapiens (human)
DOID:0050985
  • spinocerebellar ataxia type 38
Homo sapiens (human)
DOID:0050984
  • spinocerebellar ataxia type 37
Homo sapiens (human)
DOID:0050983
  • spinocerebellar ataxia type 36
Homo sapiens (human)
DOID:0050981
  • spinocerebellar ataxia type 34
Homo sapiens (human)
DOID:0050978
  • spinocerebellar ataxia type 29
Homo sapiens (human)
DOID:0050975
  • spinocerebellar ataxia type 26
Homo sapiens (human)
DOID:0050974
  • spinocerebellar ataxia type 25
Homo sapiens (human)
DOID:0050968
  • autosomal dominant cerebellar ataxia, deafness and narcolepsy
Homo sapiens (human)
DOID:0050967
  • spinocerebellar ataxia type 17
Homo sapiens (human)
DOID:0050965
  • spinocerebellar ataxia type 15
  • Aliases:
    • spinocerebellar ataxia type 16
Homo sapiens (human)
DOID:0050963
  • spinocerebellar ataxia type 13
Homo sapiens (human)
Download data in CSV format Download data in TSV format Download data in JSON format
About Release Notes Help Feedback

Click here to visit the beta site.

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

Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International

GlyCosmos Portal v4.1.0

Last updated: December 9, 2024