GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 1226 - 1250 of 4621 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism
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
Homo sapiens (human)
DOID:10930
  • borderline personality disorder
Homo sapiens (human)
DOID:10845
  • St. Louis encephalitis
  • Aliases:
    • Neuroinvasive St. Louis encephalitis virus infection
Homo sapiens (human)
DOID:11335
  • sarcoidosis
  • Aliases:
    • Boeck sarcoid
    • lymphogranulomatosis
Homo sapiens (human)
DOID:626
  • complement deficiency
  • Aliases:
    • Complement deficiency disease
Homo sapiens (human)
DOID:13003
  • vertebrobasilar insufficiency
  • Aliases:
    • Vertebro-basilar insufficiency
    • Vertebrobasilar arterial insufficiency
    • Vertebrobasilar artery syndrome
Homo sapiens (human)
DOID:4449
  • macular retinal edema
  • Aliases:
    • macular edema
    • macular oedema
    • macular retinal oedema
Homo sapiens (human)
DOID:4447
  • cystoid macular edema
Homo sapiens (human)
DOID:0060302
  • type II complement component 8 deficiency
Homo sapiens (human)
DOID:0060300
  • complement component 7 deficiency
Homo sapiens (human)
DOID:0060299
  • complement component 6 deficiency
Homo sapiens (human)
DOID:0060303
  • complement component 9 deficiency
Homo sapiens (human)
DOID:0060301
  • type I complement component 8 deficiency
Homo sapiens (human)
DOID:0060297
  • complement component 4a deficiency
Homo sapiens (human)
DOID:0060298
  • complement component 4b deficiency
Homo sapiens (human)
DOID:1742
  • drug psychosis
  • Aliases:
    • Drug-induced psychosis
    • Drug-induced psychotic disorder
Homo sapiens (human)
DOID:10272
  • left bundle branch hemiblock
  • Aliases:
    • Left bundle branch block
Homo sapiens (human)
DOID:1754
  • mitral valve stenosis
  • Aliases:
    • Mitral stenosis
Homo sapiens (human)
DOID:13404
  • uveoparotid fever
  • Aliases:
    • Heerfordt's syndrome
Homo sapiens (human)
DOID:9182
  • pemphigus
Homo sapiens (human)
DOID:0060444
  • granular corneal dystrophy 2
  • Aliases:
    • CGD2
    • avellino corneal dystrophy
    • combined granular-lattice corneal dystrophy
    • corneal dystrophy, Avellino type
    • granular corneal dystrophy type 2
Homo sapiens (human)
DOID:2733
  • skin atrophy
  • Aliases:
    • Atrophoderma
    • Atrophy - skin
    • atrophic condition of skin
Homo sapiens (human)
DOID:9719
  • neovascular inflammatory vitreoretinopathy
  • Aliases:
    • ADNIV
    • Retinitis proliferans
    • autosomal dominant neovascular inflammatory vitreoretinopathy
    • proliferative vitreoretinopathy
Homo sapiens (human)
DOID:12971
  • hereditary spherocytosis
  • Aliases:
    • Congenital spherocytic hemolytic anemia
    • Minkowski Chauffard syndrome
    • spherocytic anemia
Homo sapiens (human)
DOID:0050152
  • aspiration pneumonia
Homo sapiens (human)

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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


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Last updated: August 19, 2024