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 8126 - 8150 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲ Source
DOID:4371
  • Schnitzler syndrome
Mus musculus (house mouse)
DOID:0110117
  • autoimmune lymphoproliferative syndrome type 4
  • Aliases:
    • ALPS type 4
    • ALPS type IV
    • ALPS4
    • RALD
    • RAS-associated autoimmune leukoproliferative disease
    • RAS-associated autoimmune leukoproliferative disorder
    • autoimmune lymphoproliferative syndrome type IV
Mus musculus (house mouse)
DOID:0060468
  • Holt-Oram syndrome
  • Aliases:
    • atrio-digital syndrome
    • atriodigital dysplasia
    • heart-hand syndrome
Mus musculus (house mouse)
DOID:2527
  • nephrosis
Mus musculus (house mouse)
DOID:11450
  • allergic cutaneous vasculitis
  • Aliases:
    • Allergic Cutaneous Angiitis
    • Autoimmune Hypersensitivity angiitis
Mus musculus (house mouse)
DOID:0081030
  • central conducting lymphatic anomaly
  • Aliases:
    • lymphatic malformation-7
Mus musculus (house mouse)
DOID:906
  • peroxisomal disease
  • Aliases:
    • peroxisomal disorder
Mus musculus (house mouse)
DOID:4677
  • keratitis
Mus musculus (house mouse)
DOID:3385
  • bacterial vaginosis
Mus musculus (house mouse)
DOID:0080187
  • chronic neutrophilic leukemia
Mus musculus (house mouse)
DOID:0111279
  • psoriasis 7
  • Aliases:
    • PSORS7
Mus musculus (house mouse)
DOID:0111344
  • myeloproliferative disorder with eosinophilia
  • Aliases:
    • chronic myeloproliferative disorder with eosinophilia
Mus musculus (house mouse)
DOID:0050572
  • cone-rod dystrophy
  • Aliases:
    • cone-rod retinal dystrophy
Mus musculus (house mouse)
DOID:0070394
  • developmental and epileptic encephalopathy 108
  • Aliases:
    • DEE108
    • early infantile epileptic encephalopathy 108
Mus musculus (house mouse)
DOID:0070149
  • hereditary sensory and autonomic neuropathy type 7
  • Aliases:
    • HSAN7
    • hereditary sensory and autonomic neuropathy type VII
Mus musculus (house mouse)
DOID:13533
  • osteopetrosis
  • Aliases:
    • Albers-Schonberg disease
    • marble bone
Mus musculus (house mouse)
DOID:0112184
  • thyroid dyshormonogenesis 5
  • Aliases:
    • TDH5
    • genetic defect in thyroid hormonogenesis 5
Mus musculus (house mouse)
DOID:0080922
  • bilateral frontoparietal polymicrogyria
Mus musculus (house mouse)
DOID:0080821
  • exercise-induced bronchoconstriction
  • Aliases:
    • exercise-induced asthma
Mus musculus (house mouse)
DOID:0081034
  • glutatione synthetase deficiency with 5-oxoprolinuria
Mus musculus (house mouse)
DOID:824
  • periodontitis
  • Aliases:
    • chronic pericementitis
Mus musculus (house mouse)
DOID:0080941
  • acquired angioedema
Mus musculus (house mouse)
DOID:0081137
  • agammaglobulinemia 3
Mus musculus (house mouse)
DOID:0112127
  • HRPT-related hyperuricemia
  • Aliases:
    • HPRT deficiency, grade I
    • HPRT partial deficiency
    • HPRT-related gout
    • HPRT-related hyperuricemia
    • HPRT1 partial deficiency
    • Kelley-Seegmiller syndrome
    • hypoxanthine guanine phosphoribosyltransferase 1 partial deficiency
    • hypoxanthine guanine phosphoribosyltransferase deficiency, grade I
    • hypoxanthine guanine phosphoribosyltransferase partial deficiency
Mus musculus (house mouse)
DOID:0080026
  • otospondylomegaepiphyseal dysplasia, autosomal recessive
  • Aliases:
    • CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS
    • NANCE-INSLEY SYNDROME
    • NANCE-SWEENEY CHONDRODYSPLASIA
    • OSMEDB
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