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 July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 3326 - 3350 of 7942 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism
DOID:13317
  • hyperinsulinemic hypoglycemia
  • Aliases:
    • Islet cell hyperplasia
    • nesidioblastosis
    • persistent hyperinsulinemia hypoglycemia of infancy
Homo sapiens (human)
DOID:13317
  • hyperinsulinemic hypoglycemia
  • Aliases:
    • Islet cell hyperplasia
    • nesidioblastosis
    • persistent hyperinsulinemia hypoglycemia of infancy
Rattus norvegicus (Norway rat)
DOID:13317
  • hyperinsulinemic hypoglycemia
  • Aliases:
    • Islet cell hyperplasia
    • nesidioblastosis
    • persistent hyperinsulinemia hypoglycemia of infancy
Saccharomyces cerevisiae S288C
DOID:9279
  • hyperhomocysteinemia
Drosophila melanogaster (fruit fly)
DOID:9279
  • hyperhomocysteinemia
Rattus norvegicus (Norway rat)
DOID:9279
  • hyperhomocysteinemia
Saccharomyces cerevisiae S288C
DOID:9279
  • hyperhomocysteinemia
Caenorhabditis elegans
DOID:9279
  • hyperhomocysteinemia
Mus musculus (house mouse)
DOID:9279
  • hyperhomocysteinemia
Homo sapiens (human)
DOID:4195
  • hyperglycemia
Rattus norvegicus (Norway rat)
DOID:4195
  • hyperglycemia
Saccharomyces cerevisiae S288C
DOID:4195
  • hyperglycemia
Mus musculus (house mouse)
DOID:4195
  • hyperglycemia
Homo sapiens (human)
DOID:4195
  • hyperglycemia
Drosophila melanogaster (fruit fly)
DOID:0111256
  • hyperferritinemia-cataract syndrome
  • Aliases:
    • Bonneau-Beaumont syndrome
    • HHCS
    • HRFTC
    • cataract-hyperferritinemia syndrome
    • hereditary hyperferritinemia with congenital cataracts
    • hereditary hyperferritinemia-cataract syndrome
    • hyperferritinemia with or without cataract
Homo sapiens (human)
DOID:999
  • hypereosinophilic syndrome
  • Aliases:
    • Eosinophilic leukocytosis
    • eosinophilia
Homo sapiens (human)
DOID:0060695
  • hyperekplexia
  • Aliases:
    • Kok disease
    • congenital stiff man syndrome
    • familial startle disease
    • hereditary hyperekplexia
    • startle disease
Homo sapiens (human)
DOID:0060698
  • hyperekplexia 3
  • Aliases:
    • HKPX3
Homo sapiens (human)
DOID:0060697
  • hyperekplexia 2
  • Aliases:
    • HKPX2
Homo sapiens (human)
DOID:0060696
  • hyperekplexia 1
  • Aliases:
    • HKPX1
Homo sapiens (human)
DOID:12733
  • hypercementosis
  • Aliases:
    • Cementation hyperplasia
Homo sapiens (human)
DOID:12678
  • hypercalcemia
Homo sapiens (human)
DOID:9278
  • hyperargininemia
  • Aliases:
    • Arginase deficiency
    • argininemia
    • deficiency of canavanase
Homo sapiens (human)
DOID:11613
  • hyperandrogenism
  • Aliases:
    • hyperandrogenization syndrome
Mus musculus (house mouse)
DOID:11613
  • hyperandrogenism
  • Aliases:
    • hyperandrogenization 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: August 19, 2024