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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 8151 - 8175 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:0111686
  • hereditary mixed polyposis syndrome 2
  • Aliases:
    • HMPS2
Caenorhabditis elegans
DOID:0111686
  • hereditary mixed polyposis syndrome 2
  • Aliases:
    • HMPS2
Mus musculus (house mouse)
DOID:0111686
  • hereditary mixed polyposis syndrome 2
  • Aliases:
    • HMPS2
Homo sapiens (human)
DOID:0111683
  • neurofibromatosis-Noonan syndrome
  • Aliases:
    • NFNS
    • Noonan neurofibromatosis syndrome
    • neurofibromatosis type 1-Noonan syndrome
    • neurofibromatosis with Noonan phenotype
Mus musculus (house mouse)
DOID:0111683
  • neurofibromatosis-Noonan syndrome
  • Aliases:
    • NFNS
    • Noonan neurofibromatosis syndrome
    • neurofibromatosis type 1-Noonan syndrome
    • neurofibromatosis with Noonan phenotype
Homo sapiens (human)
DOID:0111682
  • diffuse cystic renal dysplasia
  • Aliases:
    • CYSRD
    • renal dysplasia diffuse cystic
    • susceptibility to cystic renal dysplasia
Homo sapiens (human)
DOID:0111681
  • glutamate-cysteine ligase deficiency
  • Aliases:
    • gamma-glutamylcysteine synthetase deficiency
    • hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency
Rattus norvegicus (Norway rat)
DOID:0111681
  • glutamate-cysteine ligase deficiency
  • Aliases:
    • gamma-glutamylcysteine synthetase deficiency
    • hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency
Homo sapiens (human)
DOID:0111681
  • glutamate-cysteine ligase deficiency
  • Aliases:
    • gamma-glutamylcysteine synthetase deficiency
    • hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency
Mus musculus (house mouse)
DOID:0111680
  • essential fructosuria
  • Aliases:
    • fructokinase deficiency
    • hepatic fructokinase deficiency
    • ketohexokinase deficiency
Rattus norvegicus (Norway rat)
DOID:0111680
  • essential fructosuria
  • Aliases:
    • fructokinase deficiency
    • hepatic fructokinase deficiency
    • ketohexokinase deficiency
Mus musculus (house mouse)
DOID:0111680
  • essential fructosuria
  • Aliases:
    • fructokinase deficiency
    • hepatic fructokinase deficiency
    • ketohexokinase deficiency
Homo sapiens (human)
DOID:0111678
  • hereditary folate malabsorption
  • Aliases:
    • congenital defect of folate absorption
    • congenital folate malabsorption
Danio rerio (zebrafish)
DOID:0111678
  • hereditary folate malabsorption
  • Aliases:
    • congenital defect of folate absorption
    • congenital folate malabsorption
Rattus norvegicus (Norway rat)
DOID:0111678
  • hereditary folate malabsorption
  • Aliases:
    • congenital defect of folate absorption
    • congenital folate malabsorption
Mus musculus (house mouse)
DOID:0111678
  • hereditary folate malabsorption
  • Aliases:
    • congenital defect of folate absorption
    • congenital folate malabsorption
Homo sapiens (human)
DOID:0111678
  • hereditary folate malabsorption
  • Aliases:
    • congenital defect of folate absorption
    • congenital folate malabsorption
Xenopus laevis (African clawed frog)
DOID:0111678
  • hereditary folate malabsorption
  • Aliases:
    • congenital defect of folate absorption
    • congenital folate malabsorption
Caenorhabditis elegans
DOID:0111677
  • familial benign fleck retina
  • Aliases:
    • FRFB
Homo sapiens (human)
DOID:0111676
  • high molecular weight kininogen deficiency
  • Aliases:
    • Fitzgerald trait
    • HMWK deficiency
    • congenital high-molecular-weight kininogen deficiency
Homo sapiens (human)
DOID:0111676
  • high molecular weight kininogen deficiency
  • Aliases:
    • Fitzgerald trait
    • HMWK deficiency
    • congenital high-molecular-weight kininogen deficiency
Mus musculus (house mouse)
DOID:0111676
  • high molecular weight kininogen deficiency
  • Aliases:
    • Fitzgerald trait
    • HMWK deficiency
    • congenital high-molecular-weight kininogen deficiency
Rattus norvegicus (Norway rat)
DOID:0111675
  • neurooculocardiogenitourinary syndrome
  • Aliases:
    • NOCGUS
Homo sapiens (human)
DOID:0111675
  • neurooculocardiogenitourinary syndrome
  • Aliases:
    • NOCGUS
Mus musculus (house mouse)
DOID:0111674
  • intellectual developmental disorder with short stature and behavioral abnormalities
  • Aliases:
    • IDDSSBA
Saccharomyces cerevisiae S288C
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Last updated: December 9, 2024