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 January 28, 2025
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 1 - 25 of 4115 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism Source
DOID:0001816
  • angiosarcoma
  • Aliases:
    • hemangiosarcoma
Homo sapiens (human)
DOID:0002116
  • pterygium
  • Aliases:
    • surfer's eye
Homo sapiens (human)
DOID:0014667
  • disease of metabolism
  • Aliases:
    • metabolic disease
Homo sapiens (human)
DOID:0040085
  • bacterial sepsis
Homo sapiens (human)
DOID:0040086
  • Polyomavirus-associated nephropathy
  • Aliases:
    • PVAN
    • polyomavirus associated nephropathy
Homo sapiens (human)
DOID:0040090
  • autoimmune gastritis
Homo sapiens (human)
DOID:0040091
  • autoimmune pancreatitis
Homo sapiens (human)
DOID:0050012
  • chikungunya
  • Aliases:
    • Chikungunya fever
Homo sapiens (human)
DOID:0050073
  • invasive aspergillosis
Homo sapiens (human)
DOID:0050083
  • Keshan disease
Homo sapiens (human)
DOID:0050117
  • disease by infectious agent
  • Aliases:
    • infectious disease
Homo sapiens (human)
DOID:0050127
  • sinusitis
Homo sapiens (human)
DOID:0050144
  • Kartagener syndrome
  • Aliases:
    • Kartagener's syndrome
Homo sapiens (human)
DOID:0050152
  • aspiration pneumonia
Homo sapiens (human)
DOID:0050156
  • idiopathic pulmonary fibrosis
  • Aliases:
    • FIBROCYSTIC PULMONARY DYSPLASIA
    • IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL
    • cryptogenic fibrosing alveolitis
Homo sapiens (human)
DOID:0050168
  • autoimmune polyendocrine syndrome type 2
  • Aliases:
    • Schmidt syndrome
Homo sapiens (human)
DOID:0050185
  • erythema multiforme
Homo sapiens (human)
DOID:0050211
  • swine influenza
Homo sapiens (human)
DOID:0050214
  • Lambert-Eaton myasthenic syndrome
  • Aliases:
    • Eaton-Lambert syndrome
    • LEMS
    • Lambert-Eaton syndrome
Homo sapiens (human)
DOID:0050328
  • congenital hypothyroidism
Homo sapiens (human)
DOID:0050331
  • lacrimoauriculodentodigital syndrome 1
  • Aliases:
    • LEVY-HOLLISTER SYNDROME
    • Lacrimo-auriculo-dento-digital syndrome 1
Homo sapiens (human)
DOID:0050419
  • complement factor I deficiency
  • Aliases:
    • C3 INACTIVATOR DEFICIENCY
    • COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY
Homo sapiens (human)
DOID:0050424
  • familial adenomatous polyposis
  • Aliases:
    • adenomatous polyposis of the colon
Homo sapiens (human)
DOID:0050425
  • restless legs syndrome
  • Aliases:
    • WED
    • Willis-Ekbom disease
    • Wittmaack-Ekbom syndrome
Homo sapiens (human)
DOID:0050426
  • Stevens-Johnson syndrome
Homo sapiens (human)

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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: March 31, 2025