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 5501 - 5525 of 15957 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:0050557
  • congenital muscular dystrophy
Caenorhabditis elegans
DOID:2033
  • communication disorder
Caenorhabditis elegans
DOID:0090050
  • dystonia 27
Caenorhabditis elegans
DOID:0050558
  • Ullrich congenital muscular dystrophy
  • Aliases:
    • ULLRICH DISEASE
    • Ullrich scleroatonic muscular dystrophy
Caenorhabditis elegans
DOID:0050663
  • Bethlem myopathy
  • Aliases:
    • benign congenital muscular dystrophy
Caenorhabditis elegans
DOID:13223
  • uterine fibroid
  • Aliases:
    • Plexiform leiomyoma
    • UTERUS FIBROMA
    • leiomyoma of Corpus Uteri
    • uterine leiomyoma
Caenorhabditis elegans
DOID:784
  • chronic kidney disease
  • Aliases:
    • CKD
    • CRF
    • chronic kidney failure
    • chronic renal disease
    • chronic renal failure syndrome
    • renal failure - chronic
Caenorhabditis elegans
DOID:1070
  • primary open angle glaucoma
  • Aliases:
    • chronic simple glaucoma
Caenorhabditis elegans
DOID:11054
  • urinary bladder cancer
  • Aliases:
    • bladder cancer
    • tumor of the bladder
Caenorhabditis elegans
DOID:14004
  • thoracic aortic aneurysm
Caenorhabditis elegans
DOID:10534
  • stomach cancer
  • Aliases:
    • gastric cancer
    • gastric neoplasm
Caenorhabditis elegans
DOID:8577
  • ulcerative colitis
  • Aliases:
    • Left-sided ulcerative colitis
Caenorhabditis elegans
DOID:10763
  • hypertension
  • Aliases:
    • HTN
    • hyperpiesia
    • vascular hypertensive disorder
Caenorhabditis elegans
DOID:9884
  • muscular dystrophy
Caenorhabditis elegans
DOID:653
  • purine-pyrimidine metabolic disorder
  • Aliases:
    • inborn errors of purine-pyrimidine metabolism
Caenorhabditis elegans
DOID:0050833
  • orotic aciduria
Caenorhabditis elegans
DOID:0060363
  • glycerol kinase deficiency
Caenorhabditis elegans
DOID:13810
  • familial hypercholesterolemia
  • Aliases:
    • Fredrickson type IIa hyperlipoproteinemia
    • Fredrickson type IIa lipidaemia
    • familial hyperbetalipoproteinaemia
    • familial hypercholesteremia
    • hyperbetalipoproteinemia
    • type II hyperlipidemia
Caenorhabditis elegans
DOID:0050461
  • aspartylglucosaminuria
  • Aliases:
    • aspartylglucosaminidase deficiency
    • aspartylglycosaminuria
    • glycosylasparaginase deficiency
Caenorhabditis elegans
DOID:3211
  • lysosomal storage disease
  • Aliases:
    • disorder of lysosomal enzyme
    • inborn lysosomal enzyme disorder
    • lysosomal storage metabolism disorder
Caenorhabditis elegans
DOID:0080010
  • bone structure disease
Rattus norvegicus (Norway rat)
DOID:2746
  • glycogen storage disease V
  • Aliases:
    • Glycogen storage disease 5
    • Glycogen storage disease, type V
    • McArdle's disease
    • glycogen storage disease type V
    • myophosphorylase deficiency
Mus musculus (house mouse)
DOID:2754
  • glycogen storage disease VI
  • Aliases:
    • Glycogen storage disease 6
    • Hers' disease
    • glycogen storage disease type VI
    • hepatic glycogen phosphorylase deficiency
    • hepatophosphorylase deficiency glycogenosis
Rattus norvegicus (Norway rat)
DOID:2754
  • glycogen storage disease VI
  • Aliases:
    • Glycogen storage disease 6
    • Hers' disease
    • glycogen storage disease type VI
    • hepatic glycogen phosphorylase deficiency
    • hepatophosphorylase deficiency glycogenosis
Mus musculus (house mouse)
DOID:1926
  • Gaucher's disease
  • Aliases:
    • Gaucher disease
    • acid beta-glucosidase deficiency
    • glocucerebrosidase deficiency
    • glucosylceramide beta-glucosidase deficiency
    • kerasin thesaurismosis
Drosophila melanogaster (fruit fly)

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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