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 6526 - 6550 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0080941
  • acquired angioedema
Homo sapiens (human)
DOID:0050461
  • aspartylglucosaminuria
  • Aliases:
    • aspartylglucosaminidase deficiency
    • aspartylglycosaminuria
    • glycosylasparaginase deficiency
Drosophila melanogaster (fruit fly)
DOID:0060704
  • lymphoproliferative syndrome
  • Aliases:
    • Combined immunodeficiency due to ITK deficiency
Saccharomyces cerevisiae S288C
DOID:0110444
  • dilated cardiomyopathy 1X
  • Aliases:
    • CMD1X
    • dilated cardiomyopathy with mild or no proximal muscle weakness
Caenorhabditis elegans
DOID:0050962
  • spinocerebellar ataxia type 12
Mus musculus (house mouse)
DOID:0080561
  • congenital disorder of glycosylation Ii
  • Aliases:
    • congenital disorder of glycosylation 1i
Caenorhabditis elegans
DOID:1475
  • lymphangioma
  • Aliases:
    • Congenital lymphangioma
    • benign lymphangioma
Rattus norvegicus (Norway rat)
DOID:0060684
  • autosomal dominant nocturnal frontal lobe epilepsy 3
  • Aliases:
    • ENFL3
    • nocturnal frontal lobe epilepsy 3
Rattus norvegicus (Norway rat)
DOID:7147
  • ankylosing spondylitis
  • Aliases:
    • Bekhterev syndrome
    • Bekhterev's disease
    • Marie-Strumpell disease
Danio rerio (zebrafish)
DOID:574
  • peripheral nervous system disease
Homo sapiens (human)
DOID:14764
  • Larsen syndrome
  • Aliases:
    • dominant larsen syndrome
Homo sapiens (human)
DOID:0111098
  • Fanconi anemia complementation group B
  • Aliases:
    • FACB
    • FANCB
    • Fanconi pancytopenia type 2
Homo sapiens (human)
DOID:0070072
  • autosomal dominant intellectual developmental disorder 42
  • Aliases:
    • MRD42
    • autosomal dominant mental retardation 42
    • autosomal dominant non-syndromic intellectual disability 42
Mus musculus (house mouse)
DOID:1148
  • polydactyly
  • Aliases:
    • postaxial polydactyly
Mus musculus (house mouse)
DOID:0080991
  • congenital myopathy 1B
  • Aliases:
    • multiminicore disease
Mus musculus (house mouse)
DOID:4896
  • bile duct adenocarcinoma
Homo sapiens (human)
DOID:10584
  • retinitis pigmentosa
  • Aliases:
    • pericentral pigmentary retinopathy
Caenorhabditis elegans
DOID:0111990
  • immunodeficiency 30
  • Aliases:
    • IMD30
    • MSMD due to complete IL12RB1 deficiency
    • MSMD due to complete interleukin 12 receptor beta 1 deficiency
    • Mendelian susceptibility to interleukin 12 receptor beta 1 deficiency
    • Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency
Mus musculus (house mouse)
DOID:0070405
  • hypomyelinating leukodystrophy 16
  • Aliases:
    • HLD16
Rattus norvegicus (Norway rat)
DOID:0080533
  • Carney-Stratakis syndrome
Homo sapiens (human)
DOID:0080827
  • human cytomegalovirus infection
Saccharomyces cerevisiae S288C
DOID:0111739
  • X-linked deafness 1
  • Aliases:
    • DFN2
    • DFNX1
    • X-linked sensorineural congenital deafness 2
Mus musculus (house mouse)
DOID:14018
  • alcoholic liver cirrhosis
  • Aliases:
    • Alcoholic Cirrhosis
    • Alcoholic cirrhosis of liver
    • Laennec's cirrhosis
    • Laennec's cirrhosis, alcoholic
    • Portal cirrhosis
Rattus norvegicus (Norway rat)
DOID:0111029
  • hemochromatosis type 1
  • Aliases:
    • HFE1
    • symptomatic form of HFE-related hereditary hemochromatosis
    • symptomatic form of classic hemochromatosis
    • symptomatic form of hemochromatosis type 1
Mus musculus (house mouse)
DOID:0081188
  • autosomal recessive intellectual developmental disorder 14
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