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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 1401 - 1425 of 4649 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▲
DOID:0080860
  • primary ovarian insufficiency 3
Homo sapiens (human)
DOID:0080862
  • primary ovarian insufficiency 5
Homo sapiens (human)
DOID:0080865
  • primary ovarian insufficiency 8
Homo sapiens (human)
DOID:0080866
  • primary ovarian insufficiency 9
Homo sapiens (human)
DOID:0080868
  • primary ovarian insufficiency 11
Homo sapiens (human)
DOID:0080871
  • primary ovarian insufficiency 14
Homo sapiens (human)
DOID:0080872
  • primary ovarian insufficiency 15
Homo sapiens (human)
DOID:0080886
  • vitamin D-dependent rickets type 1A
Homo sapiens (human)
DOID:0080887
  • vitamin D-dependent rickets type 1B
Homo sapiens (human)
DOID:0080893
  • Bainbridge-Ropers syndrome
  • Aliases:
    • ASXL3-related disorder
Homo sapiens (human)
DOID:0080899
  • lung pleomorphic carcinoma
Homo sapiens (human)
DOID:0080908
  • Cockayne syndrome B
  • Aliases:
    • Cockayne syndrome 2
    • Cockayne syndrome type II
Homo sapiens (human)
DOID:0080909
  • castration-resistant prostate carcinoma
Homo sapiens (human)
DOID:0080911
  • cerebrooculofacioskeletal syndrome 1
Homo sapiens (human)
DOID:0080913
  • cerebrooculofacioskeletal syndrome 3
Homo sapiens (human)
DOID:0080918
  • polymicrogyria
Homo sapiens (human)
DOID:0080922
  • bilateral frontoparietal polymicrogyria
Homo sapiens (human)
DOID:0080923
  • bilateral parasagittal parieto-occipital polymicrogyria
  • Aliases:
    • bilateral temporooccipital polymicrogyria
Homo sapiens (human)
DOID:0080924
  • bilateral perisylvian polymicrogyria
Homo sapiens (human)
DOID:0080925
  • cytochrome P450 oxidoreductase deficiency
Homo sapiens (human)
DOID:0080930
  • primary localized cutaneous amyloidosis 1
  • Aliases:
    • familial primary localized cutaneous amyloidosis-1
Homo sapiens (human)
DOID:0080931
  • primary localized cutaneous amyloidosis 2
Homo sapiens (human)
DOID:0080932
  • primary localized cutaneous amyloidosis 3
  • Aliases:
    • Amyloidosis cutis dyschromica
Homo sapiens (human)
DOID:0080933
  • immunoglobulin light chain amyloidosis
  • Aliases:
    • AL amyloidosis
    • Amyloidosis primary systemic
    • Light chain amyloidosis
    • Primary AL amyloidosis
    • Primary systemic AL amyloidosis
    • Primary systemic amyloidosis
    • Systemic AL amyloidsis
Homo sapiens (human)
DOID:0080939
  • hereditary angioedema type I
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: December 9, 2024