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 13551 - 13575 of 15957 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism Source
DOID:0070238
  • primary coenzyme Q10 deficiency 1
  • Aliases:
    • COQ10D1
    • CoQ deficiency 1
    • CoQ10 deficiency, primary, 1
    • coenzyme Q deficiency 1
    • ubiquinone deficiency 1
Homo sapiens (human)
DOID:0070238
  • primary coenzyme Q10 deficiency 1
  • Aliases:
    • COQ10D1
    • CoQ deficiency 1
    • CoQ10 deficiency, primary, 1
    • coenzyme Q deficiency 1
    • ubiquinone deficiency 1
Rattus norvegicus (Norway rat)
DOID:0070238
  • primary coenzyme Q10 deficiency 1
  • Aliases:
    • COQ10D1
    • CoQ deficiency 1
    • CoQ10 deficiency, primary, 1
    • coenzyme Q deficiency 1
    • ubiquinone deficiency 1
Mus musculus (house mouse)
DOID:0070241
  • primary coenzyme Q10 deficiency 4
  • Aliases:
    • COQ10D4
    • SCAR9
    • coenzyme Q10 deficiency, primary, 4
    • spinocerebellar ataxia, autosomal recessive 9
Rattus norvegicus (Norway rat)
DOID:0070242
  • primary coenzyme Q10 deficiency 5
  • Aliases:
    • COQ10D5
    • coenzyme Q10 deficiency, primary, 5
    • encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome
Mus musculus (house mouse)
DOID:0070242
  • primary coenzyme Q10 deficiency 5
  • Aliases:
    • COQ10D5
    • coenzyme Q10 deficiency, primary, 5
    • encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome
Homo sapiens (human)
DOID:0070243
  • primary coenzyme Q10 deficiency 6
  • Aliases:
    • COQ10D6
    • coenzyme Q10 deficiency, primary, 6
    • familial steroid-resistant nephrotic syndrome with sensorineural deafness
Homo sapiens (human)
DOID:0050593
  • primary congenital glaucoma
Homo sapiens (human)
DOID:0060061
  • primary cutaneous T-cell non-Hodgkin lymphoma
  • Aliases:
    • cutaneous T cell lymphoma
    • cutaneous T-cell lymphoma
Mus musculus (house mouse)
DOID:0060061
  • primary cutaneous T-cell non-Hodgkin lymphoma
  • Aliases:
    • cutaneous T cell lymphoma
    • cutaneous T-cell lymphoma
Rattus norvegicus (Norway rat)
DOID:0060061
  • primary cutaneous T-cell non-Hodgkin lymphoma
  • Aliases:
    • cutaneous T cell lymphoma
    • cutaneous T-cell lymphoma
Homo sapiens (human)
DOID:0050639
  • primary cutaneous amyloidosis
  • Aliases:
    • PCA
    • familial primary localized cutaneous amyloidosis
Homo sapiens (human)
DOID:0111341
  • primary failure of tooth eruption
  • Aliases:
    • PFE
    • dental noneruption
    • familial posterior openbite malocclusion
    • nonsyndromic primary failure of eruption
    • primary retention of teeth
    • unerupted second primary molar
Homo sapiens (human)
DOID:0111341
  • primary failure of tooth eruption
  • Aliases:
    • PFE
    • dental noneruption
    • familial posterior openbite malocclusion
    • nonsyndromic primary failure of eruption
    • primary retention of teeth
    • unerupted second primary molar
Mus musculus (house mouse)
DOID:0111341
  • primary failure of tooth eruption
  • Aliases:
    • PFE
    • dental noneruption
    • familial posterior openbite malocclusion
    • nonsyndromic primary failure of eruption
    • primary retention of teeth
    • unerupted second primary molar
Rattus norvegicus (Norway rat)
DOID:0111341
  • primary failure of tooth eruption
  • Aliases:
    • PFE
    • dental noneruption
    • familial posterior openbite malocclusion
    • nonsyndromic primary failure of eruption
    • primary retention of teeth
    • unerupted second primary molar
Caenorhabditis elegans
DOID:446
  • primary hyperaldosteronism
  • Aliases:
    • Cushing syndrome
    • Cushing's syndrome
    • hyperaldosteronism
Caenorhabditis elegans
DOID:446
  • primary hyperaldosteronism
  • Aliases:
    • Cushing syndrome
    • Cushing's syndrome
    • hyperaldosteronism
Danio rerio (zebrafish)
DOID:446
  • primary hyperaldosteronism
  • Aliases:
    • Cushing syndrome
    • Cushing's syndrome
    • hyperaldosteronism
Saccharomyces cerevisiae S288C
DOID:446
  • primary hyperaldosteronism
  • Aliases:
    • Cushing syndrome
    • Cushing's syndrome
    • hyperaldosteronism
Mus musculus (house mouse)
DOID:446
  • primary hyperaldosteronism
  • Aliases:
    • Cushing syndrome
    • Cushing's syndrome
    • hyperaldosteronism
Drosophila melanogaster (fruit fly)
DOID:446
  • primary hyperaldosteronism
  • Aliases:
    • Cushing syndrome
    • Cushing's syndrome
    • hyperaldosteronism
Homo sapiens (human)
DOID:446
  • primary hyperaldosteronism
  • Aliases:
    • Cushing syndrome
    • Cushing's syndrome
    • hyperaldosteronism
Rattus norvegicus (Norway rat)
DOID:0111670
  • primary hyperoxaluria type 1
  • Aliases:
    • HP1
    • alanine-glyoxylate aminotransferase deficiency
    • glycolic aciduria
    • hepatic AGT deficiency
    • oxalosis I
    • peroxisomal alanine-glyoxylate aminotransferase deficiency
    • serine pyruvate aminotransferase deficiency
Homo sapiens (human)
DOID:0111671
  • primary hyperoxaluria type 2
  • Aliases:
    • D-glycerate dehydrogenase deficiency
    • HP2
    • L-glyceric aciduria
    • glyoxylate reductase/hydroxypyruvate reductase deficiency
    • oxalosis II
Mus musculus (house mouse)
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