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 9376 - 9400 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:0110433
  • dilated cardiomyopathy 1E
  • Aliases:
    • CDCD2
    • CMD1E
    • dilated cardiomyopathy with conduction defect 2
    • dilated cardiomyopathy with conduction disorder and arrhythmia
Mus musculus (house mouse)
DOID:0081424
  • familial focal epilepsy with variable foci 4
Mus musculus (house mouse)
DOID:0080420
  • developmental and epileptic encephalopathy 62
  • Aliases:
    • DEE62
    • early infantile epileptic encephalopathy 62
Mus musculus (house mouse)
DOID:0110222
  • Brugada syndrome 5
  • Aliases:
    • BRGDA5
Mus musculus (house mouse)
DOID:0080455
  • developmental and epileptic encephalopathy 52
  • Aliases:
    • DEE52
    • early infantile epileptic encephalopathy 52
Mus musculus (house mouse)
DOID:0111302
  • generalized epilepsy with febrile seizures plus 1
  • Aliases:
    • GEFS+1
    • GEFSP1
    • generalised epilepsy with febrile seizures plus 1
    • generalised epilepsy with febrile seizures plus type 1
    • generalized epilepsy with febrile seizures plus type 1
Mus musculus (house mouse)
DOID:0070379
  • developmental and epileptic encephalopathy 6B
  • Aliases:
    • DEE6B
Mus musculus (house mouse)
DOID:0111183
  • familial hemiplegic migraine 3
  • Aliases:
    • FHM3
    • MHP3
Mus musculus (house mouse)
DOID:0111730
  • familial episodic pain syndrome 2
  • Aliases:
    • FEPS2
Mus musculus (house mouse)
DOID:1800
  • neuroendocrine carcinoma
Homo sapiens (human)
DOID:12783
  • migraine without aura
  • Aliases:
    • common migraine
Homo sapiens (human)
DOID:0050955
  • spinocerebellar ataxia type 2
Mus musculus (house mouse)
DOID:0050954
  • spinocerebellar ataxia type 1
Mus musculus (house mouse)
DOID:12466
  • secondary hyperparathyroidism
Homo sapiens (human)
DOID:1270
  • hereditary hemorrhagic telangiectasia
  • Aliases:
    • Osler hemorrhagic telangiectasia syndrome
    • Osler-Weber-Rendu disease
    • Rendu-Osler-Weber disease
Homo sapiens (human)
DOID:0060688
  • arteriovenous malformations of the brain
  • Aliases:
    • cerebral arteriovenous malformation
    • intracranial arteriovenous malformation
Homo sapiens (human)
DOID:1037
  • lymphoid leukemia
  • Aliases:
    • lymphoblastic leukaemia
    • lymphoblastic leukemia
    • lymphocytic leukaemia
Homo sapiens (human)
DOID:0060675
  • catecholaminergic polymorphic ventricular tachycardia 1
  • Aliases:
    • CVPT1
    • arrhythmogenic right ventricular dysplasia 2
Mus musculus (house mouse)
DOID:0080991
  • congenital myopathy 1B
  • Aliases:
    • multiminicore disease
Mus musculus (house mouse)
DOID:0080990
  • King Denborough syndrome
Mus musculus (house mouse)
DOID:13100
  • intracranial vasospasm
Mus musculus (house mouse)
DOID:3529
  • congenital myopathy 1A
  • Aliases:
    • central core disease
    • central core myopathy
Mus musculus (house mouse)
DOID:0080573
  • congenital disorder of glycosylation Ix
  • Aliases:
    • congenital disorder of glycosylation 1x
Homo sapiens (human)
DOID:0080572
  • congenital disorder of glycosylation Iw
  • Aliases:
    • congenital disorder of glycosylation 1w
Homo sapiens (human)
DOID:0080386
  • nephrotic syndrome type 10
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