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 4426 - 4450 of 7942 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism
DOID:11823
  • hepatorenal syndrome
Mus musculus (house mouse)
DOID:11823
  • hepatorenal syndrome
Homo sapiens (human)
DOID:11823
  • hepatorenal syndrome
Rattus norvegicus (Norway rat)
DOID:14735
  • hereditary angioedema
  • Aliases:
    • HANE
    • Hereditary angioneurotic edema
Rattus norvegicus (Norway rat)
DOID:14735
  • hereditary angioedema
  • Aliases:
    • HANE
    • Hereditary angioneurotic edema
Xenopus laevis (African clawed frog)
DOID:14735
  • hereditary angioedema
  • Aliases:
    • HANE
    • Hereditary angioneurotic edema
Caenorhabditis elegans
DOID:14735
  • hereditary angioedema
  • Aliases:
    • HANE
    • Hereditary angioneurotic edema
Homo sapiens (human)
DOID:14735
  • hereditary angioedema
  • Aliases:
    • HANE
    • Hereditary angioneurotic edema
Xenopus tropicalis (tropical clawed frog)
DOID:14735
  • hereditary angioedema
  • Aliases:
    • HANE
    • Hereditary angioneurotic edema
Drosophila melanogaster (fruit fly)
DOID:14735
  • hereditary angioedema
  • Aliases:
    • HANE
    • Hereditary angioneurotic edema
Mus musculus (house mouse)
DOID:14735
  • hereditary angioedema
  • Aliases:
    • HANE
    • Hereditary angioneurotic edema
Danio rerio (zebrafish)
DOID:0111582
  • hereditary arterial and articular multiple calcification syndrome
  • Aliases:
    • CALJA
    • arterial calcification and distal joint calcification
    • arterial calcification due to CD73 deficiency
    • arterial calcification due to deficiency of CD73
    • calcification of joints and arteries
Homo sapiens (human)
DOID:0050951
  • hereditary ataxia
Homo sapiens (human)
DOID:5683
  • hereditary breast ovarian cancer syndrome
  • Aliases:
    • BRCA1- and BRCA2-associated hereditary breast and ovarian cancer
    • Breast and Ovarian Cancer syndrome
    • HBOC syndrome
    • Hereditary Breast and Ovarian Cancer syndrome
    • Hereditary breast and ovarian cancer
Homo sapiens (human)
DOID:13269
  • hereditary coproporphyria
  • Aliases:
    • Coproporphyrinogen oxidase deficiency
    • hereditary coproporphyria porphyria
Homo sapiens (human)
DOID:2373
  • hereditary elliptocytosis
  • Aliases:
    • Congenital elliptocytosis
    • ovalocytosis
Homo sapiens (human)
DOID:9869
  • hereditary fructose intolerance syndrome
  • Aliases:
    • Fructosaemia
    • Fructose-1,6-bisphosphate aldolase B deficiency
    • Fructosemia
Caenorhabditis elegans
DOID:9869
  • hereditary fructose intolerance syndrome
  • Aliases:
    • Fructosaemia
    • Fructose-1,6-bisphosphate aldolase B deficiency
    • Fructosemia
Mus musculus (house mouse)
DOID:9869
  • hereditary fructose intolerance syndrome
  • Aliases:
    • Fructosaemia
    • Fructose-1,6-bisphosphate aldolase B deficiency
    • Fructosemia
Danio rerio (zebrafish)
DOID:9869
  • hereditary fructose intolerance syndrome
  • Aliases:
    • Fructosaemia
    • Fructose-1,6-bisphosphate aldolase B deficiency
    • Fructosemia
Homo sapiens (human)
DOID:9869
  • hereditary fructose intolerance syndrome
  • Aliases:
    • Fructosaemia
    • Fructose-1,6-bisphosphate aldolase B deficiency
    • Fructosemia
Drosophila melanogaster (fruit fly)
DOID:1270
  • hereditary hemorrhagic telangiectasia
  • Aliases:
    • Osler hemorrhagic telangiectasia syndrome
    • Osler-Weber-Rendu disease
    • Rendu-Osler-Weber disease
Rattus norvegicus (Norway rat)
DOID:1270
  • hereditary hemorrhagic telangiectasia
  • Aliases:
    • Osler hemorrhagic telangiectasia syndrome
    • Osler-Weber-Rendu disease
    • Rendu-Osler-Weber disease
Mus musculus (house mouse)
DOID:1270
  • hereditary hemorrhagic telangiectasia
  • Aliases:
    • Osler hemorrhagic telangiectasia syndrome
    • Osler-Weber-Rendu disease
    • Rendu-Osler-Weber disease
Homo sapiens (human)
DOID:0070212
  • hereditary lymphedema I
  • Aliases:
    • LMPH1
    • Milroy disease
    • Nonne-Milroy lymphedema
    • PCL
    • congenital primary lymphedema
    • hereditary lymphedema type I
Homo sapiens (human)

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Last updated: August 19, 2024