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 15776 - 15800 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0111530
  • linear nevus sebaceous syndrome
  • Aliases:
    • JNP
    • Jadassohn nevus phakomatosis
    • SFM syndrome
    • Schimmelpenning Feuerstein Mims syndrome
    • Schimmelpenning syndrome
    • Solomon syndrome
    • nevus sebaceus of Jadassohn
    • nevus sebaceus syndrome
    • organoid nevus phakomatosis
    • organoid nevus syndrome
Homo sapiens (human)
DOID:12098
  • trigeminal neuralgia
  • Aliases:
    • Trifacial neuralgia
    • trifocal neuralgia
Rattus norvegicus (Norway rat)
DOID:0060404
  • chromosome 17q12 deletion syndrome
  • Aliases:
    • 17q12 microdeletion syndrome
Homo sapiens (human)
DOID:0110637
  • muscular dystrophy-dystroglycanopathy type B6
  • Aliases:
    • MDC1D
    • MDDGB6
    • congenital muscular dystrophy LARGE-related
    • congenital muscular dystrophy type 1D
    • muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6
    • muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 6
Homo sapiens (human)
DOID:0060696
  • hyperekplexia 1
  • Aliases:
    • HKPX1
Caenorhabditis elegans
DOID:0112219
  • developmental and epileptic encephalopathy 84
  • Aliases:
    • DEE84
    • Jamuar syndrome
    • early infantile epileptic encephalopathy 84
Mus musculus (house mouse)
DOID:1681
  • heart septal defect
  • Aliases:
    • Cardiac septal defects
    • Congenital septal defect of heart
    • septal defect
Caenorhabditis elegans
DOID:0060178
  • familial hemiplegic migraine
Drosophila melanogaster (fruit fly)
DOID:6212
  • ovarian endometrial cancer
  • Aliases:
    • endometrioid neoplasm of Ovary
    • malignant ovarian endometrioid tumor
    • ovarian endometrioid neoplasm
Mus musculus (house mouse)
DOID:10808
  • gastric ulcer
  • Aliases:
    • acute gastric ulcer with haemorrhage and perforation
    • acute gastric ulcer with hemorrhage AND with perforation but without obstruction
    • acute gastric ulcer with hemorrhage and obstruction
    • acute gastric ulcer with hemorrhage and perforation
    • acute gastric ulcer with hemorrhage and perforation, with obstruction
    • acute gastric ulcer with hemorrhage and perforation, without mention of obstruction
    • acute gastric ulcer with hemorrhage, with obstruction
    • acute gastric ulcer with hemorrhage, with perforation AND with obstruction
    • acute gastric ulcer with perforation
    • acute gastric ulcer with perforation AND obstruction
    • acute gastric ulcer with perforation, with obstruction
    • acute gastric ulcer without hemorrhage and without perforation
    • acute gastric ulcer without hemorrhage, without perforation AND without obstruction
    • acute gastric ulcer without mention of hemorrhage or perforation, without mention of obstruction
    • bleeding acute gastric ulcer
    • chronic gastric ulcer without hemorrhage AND without perforation
    • chronic gastric ulcer without hemorrhage AND without perforation but with obstruction
    • chronic gastric ulcer without mention of hemorrhage or perforation, with obstruction
Saccharomyces cerevisiae S288C
DOID:0060387
  • chondrodysplasia Blomstrand type
  • Aliases:
    • Blomstrand lethal chondrodysplasia
Homo sapiens (human)
DOID:0080444
  • developmental and epileptic encephalopathy 27
  • Aliases:
    • DEE27
    • early infantile epileptic encephalopathy 27
Rattus norvegicus (Norway rat)
DOID:2841
  • asthma
  • Aliases:
    • bronchial hyperreactivity
    • chronic obstructive asthma
    • chronic obstructive asthma with acute exacerbation
    • chronic obstructive asthma with status asthmaticus
Xenopus tropicalis (tropical clawed frog)
DOID:0050855
  • renal fibrosis
Rattus norvegicus (Norway rat)
DOID:2773
  • contact dermatitis
  • Aliases:
    • Contact dermatitis/eczema
    • Contact eczema
    • Dermatitis, venenata
    • dermatitis venenata
Rattus norvegicus (Norway rat)
DOID:2741
  • bilirubin metabolic disorder
  • Aliases:
    • hereditary hyperbilirubinemia
    • hyperbilirubinemia
Xenopus tropicalis (tropical clawed frog)
DOID:2228
  • thrombocytosis
  • Aliases:
    • Thrombocythaemia
Rattus norvegicus (Norway rat)
DOID:0090078
  • hypogonadotropic hypogonadism 7 with or without anosmia
Xenopus laevis (African clawed frog)
DOID:0111729
  • familial episodic pain syndrome 1
  • Aliases:
    • FEPS1
Rattus norvegicus (Norway rat)
DOID:0050566
  • X-linked nonsyndromic deafness
  • Aliases:
    • X-linked deafness
Mus musculus (house mouse)
DOID:0081368
  • Paget's disease of bone 5
  • Aliases:
    • Familial osteoectasia
    • Hereditary hyperphosphatasia
    • Hyperostosis corticalis deformans juvenilis
    • Juvenile Paget disease
    • Paget disease of bone-5
Mus musculus (house mouse)
DOID:0070269
  • congenital disorder of glycosylation type IIq
  • Aliases:
    • CDG IIq
    • CDG2Q
    • CDGIIdq
    • COG2-CDG
    • COG2-related congenital disorder of glycosylation
Homo sapiens (human)
DOID:12689
  • acoustic neuroma
  • Aliases:
    • Vestibular Neurilemmoma
    • Vestibular schwannoma
Homo sapiens (human)
DOID:10966
  • lipoid nephrosis
  • Aliases:
    • Minimal Change Glomerulonephritis
    • Minimal change disease
    • Nephrotic syndrome with lesion of minimal change glomerulonephritis
    • Nephrotic syndrome with lesion of minimal change nephrotic syndrome
Mus musculus (house mouse)
DOID:0110909
  • inflammatory bowel disease 25
  • Aliases:
    • IBD25
    • early onset autosomal recessive inflammatory bowel disease 25
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