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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 8576 - 8600 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0060162
  • dentatorubral-pallidoluysian atrophy
  • Aliases:
    • DRPLA
    • Haw River Syndrome
    • Naito-Oyanagi disease
Homo sapiens (human)
DOID:12140
  • Chagas disease
  • Aliases:
    • Chagas' disease
    • chagas' disease with digestive system involvement
    • chagas' disease with nervous system involvement
    • chagas' disease with other organ involvement
Rattus norvegicus (Norway rat)
DOID:0112378
  • muscular dystrophy-dystroglycanopathy type B3
  • Aliases:
    • MDDGB3
    • congenital muscular dystrophy POMGNT1-related
Danio rerio (zebrafish)
DOID:0080082
  • nonsyndromic congenital nail disorder 4
  • Aliases:
    • HYPONYCHIA CONGENITA
    • anonychia congenita
Homo sapiens (human)
DOID:0050570
  • congenital disorder of glycosylation type I
Saccharomyces cerevisiae S288C
DOID:0110429
  • dilated cardiomyopathy 1H
  • Aliases:
    • dilated cardiomyopathy with conduction defect
Rattus norvegicus (Norway rat)
DOID:5212
  • congenital disorder of glycosylation
  • Aliases:
    • carbohydrate-deficient glycoprotein syndrome
Rattus norvegicus (Norway rat)
DOID:0050424
  • familial adenomatous polyposis
  • Aliases:
    • adenomatous polyposis of the colon
Mus musculus (house mouse)
DOID:0080380
  • nephrotic syndrome type 5
  • Aliases:
    • nephrotic syndrome type 5, with or without ocular abnormalities
Caenorhabditis elegans
DOID:0060475
  • myoclonic-atonic epilepsy
  • Aliases:
    • EEOC
    • childhood onset epileptic encephalopathy
Saccharomyces cerevisiae S288C
DOID:12858
  • Huntington's disease
  • Aliases:
    • HD
    • Huntington disease
    • Huntington's chorea
Xenopus tropicalis (tropical clawed frog)
DOID:0112061
  • immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia
  • Aliases:
    • IMD73B
Homo sapiens (human)
DOID:0111390
  • mucopolysaccharidosis Ih
  • Aliases:
    • Dysostosis multiplex syndrome
    • Hurler disease MPS type 1H
    • Hurler-Pfaundler syndrome
    • L-iduronidase deficiency, Hurler type
    • MPS1-H
    • Mucopolysaccharidosis type I severe form
    • dysostosis multiplex
    • gargoylism
Drosophila melanogaster (fruit fly)
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
Homo sapiens (human)
DOID:0080312
  • neurodevelopmental disorder with midbrain and hindbrain malformations
  • Aliases:
    • NEDMHM
Homo sapiens (human)
DOID:0111028
  • hemochromatosis type 4
  • Aliases:
    • HFE4
    • autosomal dominant hereditary hemochromatosis
    • ferroportin disease
    • hemochromatosis due to defect in ferroportin
Mus musculus (house mouse)
DOID:0111235
  • congenital muscular dystrophy-dystroglycanopathy type A12
  • Aliases:
    • MDDGA12
    • Walker-Warburg syndrome or muscle-eye-brain disease POMK-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A12
Rattus norvegicus (Norway rat)
DOID:0050921
  • pharynx squamous cell carcinoma
Homo sapiens (human)
DOID:8634
  • prostate carcinoma in situ
  • Aliases:
    • PIN III
    • carcinoma in situ of prostate
    • grade III PIN
Rattus norvegicus (Norway rat)
DOID:0110765
  • hereditary spastic paraplegia 12
  • Aliases:
    • SPG12
    • autosomal dominant spastic paraplegia 12
    • autosomal dominant spastic paraplegia type 12
Mus musculus (house mouse)
DOID:14764
  • Larsen syndrome
  • Aliases:
    • dominant larsen syndrome
Mus musculus (house mouse)
DOID:0070433
  • hyperphosphatasia with impaired intellectual development syndrome 1
  • Aliases:
    • GPIBD2
    • HPMRS1
    • glycosylphosphatidylinositol biosynthesis defect 2
    • hyperphosphatasia with mental retardation syndrome 1
Caenorhabditis elegans
DOID:13378
  • Kawasaki disease
  • Aliases:
    • Kawasaki's disease
    • MLNS
    • acute febrile MCLS
    • acute febrile mucocutaneous lymph node syndrome
    • mucocutaneous lymph node syndrome
Caenorhabditis elegans
DOID:0112166
  • autosomal dominant nonsyndromic deafness 75
  • Aliases:
    • DFNA75
Homo sapiens (human)
DOID:3345
  • xanthomatosis
  • Aliases:
    • xanthelasmatosis
Homo sapiens (human)
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024