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 251 - 275 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:0080721
  • calvarial doughnut lesions with bone fragility
Homo sapiens (human)
DOID:0060480
  • left ventricular noncompaction
  • Aliases:
    • left ventricular hypertrabeculation
Homo sapiens (human)
DOID:0110045
  • Alzheimer's disease 12
  • Aliases:
    • AD12
    • Alzheimer disease 12
    • Alzheimer disease familial 12
Homo sapiens (human)
DOID:11650
  • bronchopulmonary dysplasia
  • Aliases:
    • Bronchopulmonary dysplasia of newborn
    • Chronic lung disease of prematurity
    • Neonatal chronic lung disease
    • Perinatal bronchopulmonary dysplasia
    • Respiratory insufficiency
    • neonatal chronic respiratory disease
Homo sapiens (human)
DOID:3557
  • superior mesenteric artery syndrome
  • Aliases:
    • Wilkie's syndrome
Homo sapiens (human)
DOID:11247
  • disseminated intravascular coagulation
  • Aliases:
    • DIC
    • Defibrination syndrome
    • Diffuse or disseminated intravascular coagulation
Homo sapiens (human)
DOID:14796
  • Dubowitz syndrome
  • Aliases:
    • Dubowitz's syndrome
Homo sapiens (human)
DOID:0110534
  • autosomal recessive nonsyndromic deafness 89
  • Aliases:
    • DFNB89
    • autosomal recessive deafness 89
Homo sapiens (human)
DOID:0110549
  • autosomal dominant nonsyndromic deafness 18
  • Aliases:
    • DFNA18
    • autosomal dominant deafness 18
Homo sapiens (human)
DOID:0060586
  • Noonan syndrome 8
  • Aliases:
    • NS8
Homo sapiens (human)
DOID:6873
  • skin tag
  • Aliases:
    • Fibroepithelial polyp
    • Fibroepithelial polyp of skin
    • cutaneous tag
    • soft fibroma
Homo sapiens (human)
DOID:0110522
  • autosomal recessive nonsyndromic deafness 71
  • Aliases:
    • DFNB71
    • autosomal recessive deafness 71
Homo sapiens (human)
DOID:8929
  • atrophic gastritis
  • Aliases:
    • gastric atrophy
Homo sapiens (human)
DOID:12206
  • dengue hemorrhagic fever
  • Aliases:
    • DHF
Homo sapiens (human)
DOID:14320
  • generalized anxiety disorder
Homo sapiens (human)
DOID:0080737
  • Ehlers-Danlos syndrome musculocontractural type 2
Homo sapiens (human)
DOID:11801
  • protein-energy malnutrition
Homo sapiens (human)
DOID:0070298
  • multiple epiphyseal dysplasia 2
  • Aliases:
    • EDM2
Homo sapiens (human)
DOID:0060174
  • GABA aminotransferase deficiency
  • Aliases:
    • Gamma-amino butyric acid transaminase deficiency
    • gamma-aminobutyric acid transaminase deficiency
Homo sapiens (human)
DOID:11603
  • infant gynecomastia
  • Aliases:
    • Neonatal gynaecomastia
    • breast engorgement in newborn
Homo sapiens (human)
DOID:0081243
  • rhizomelic chondrodysplasia punctate type 4
Homo sapiens (human)
DOID:5813
  • purine nucleoside phosphorylase deficiency
  • Aliases:
    • PNP deficiency
    • Purine-Nucleoside Phosphorylase deficiency
    • deficiency of inosine phosphorylase
Homo sapiens (human)
DOID:2848
  • obsolete melancholia
Homo sapiens (human)
DOID:0110432
  • dilated cardiomyopathy 1NN
  • Aliases:
    • CMD1NN
Homo sapiens (human)
DOID:0080102
  • congenital myopathy 4A
  • Aliases:
    • CFTD
    • congenital fiber-type disproportion
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: August 19, 2024