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 1376 - 1400 of 4649 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▲
DOID:0080785
  • Brown-Vialetto-Van Laere syndrome 1
Homo sapiens (human)
DOID:0080786
  • Brown-Vialetto-Van Laere syndrome 2
Homo sapiens (human)
DOID:0080787
  • proximal symphalangism 1
Homo sapiens (human)
DOID:0080788
  • proximal symphalangism 2
Homo sapiens (human)
DOID:0080789
  • Treacher Collins syndrome 1
Homo sapiens (human)
DOID:0080792
  • Treacher Collins syndrome 4
Homo sapiens (human)
DOID:0080797
  • nasal type extranodal NK/T-cell lymphoma
Homo sapiens (human)
DOID:0080799
  • sinonasal undifferentiated carcinoma
Homo sapiens (human)
DOID:0080804
  • cranioectodermal dysplasia 2
Homo sapiens (human)
DOID:0080807
  • autosomal dominant craniodiaphyseal dysplasia
Homo sapiens (human)
DOID:0080809
  • chronic asthma
Homo sapiens (human)
DOID:0080820
  • occupational asthma
Homo sapiens (human)
DOID:0080821
  • exercise-induced bronchoconstriction
  • Aliases:
    • exercise-induced asthma
Homo sapiens (human)
DOID:0080822
  • aspirin-induced respiratory disease
  • Aliases:
    • aspirin-sensitive asthma
Homo sapiens (human)
DOID:0080827
  • human cytomegalovirus infection
Homo sapiens (human)
DOID:0080828
  • VEXAS syndrome
  • Aliases:
    • vacuoles, E1 enzyme, X-linked, autoinflammatory and somatic syndrome
Homo sapiens (human)
DOID:0080832
  • mild cognitive impairment
Homo sapiens (human)
DOID:0080836
  • growth hormone insensitivity syndrome with immune dysregulation 1
Homo sapiens (human)
DOID:0080837
  • growth hormone insensitivity syndrome with immune dysregulation 2
Homo sapiens (human)
DOID:0080839
  • X-linked warfarin sensitivity
Homo sapiens (human)
DOID:0080844
  • omodysplasia 1
Homo sapiens (human)
DOID:0080845
  • omodysplasia 2
Homo sapiens (human)
DOID:0080846
  • latent autoimmune diabetes in adults
  • Aliases:
    • LADA
    • type 1.5 diabetes
Homo sapiens (human)
DOID:0080855
  • Parkinsonism
Homo sapiens (human)
DOID:0080857
  • primary ovarian insufficiency 1
  • Aliases:
    • FMR1-related primary ovarian insufficiency
    • Fragile X-associated primary ovarian insufficiency
    • premature ovarian failure 1
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: December 9, 2024