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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 6901 - 6925 of 15957 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism Source
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
Caenorhabditis elegans
DOID:2373
  • hereditary elliptocytosis
  • Aliases:
    • Congenital elliptocytosis
    • ovalocytosis
Drosophila melanogaster (fruit fly)
DOID:2373
  • hereditary elliptocytosis
  • Aliases:
    • Congenital elliptocytosis
    • ovalocytosis
Mus musculus (house mouse)
DOID:2373
  • hereditary elliptocytosis
  • Aliases:
    • Congenital elliptocytosis
    • ovalocytosis
Rattus norvegicus (Norway rat)
DOID:2373
  • hereditary elliptocytosis
  • Aliases:
    • Congenital elliptocytosis
    • ovalocytosis
Caenorhabditis elegans
DOID:2373
  • hereditary elliptocytosis
  • Aliases:
    • Congenital elliptocytosis
    • ovalocytosis
Homo sapiens (human)
DOID:0080764
  • hereditary diffuse gastric cancer
Homo sapiens (human)
DOID:0080764
  • hereditary diffuse gastric cancer
Danio rerio (zebrafish)
DOID:0080764
  • hereditary diffuse gastric cancer
Rattus norvegicus (Norway rat)
DOID:0080764
  • hereditary diffuse gastric cancer
Mus musculus (house mouse)
DOID:0080764
  • hereditary diffuse gastric cancer
Xenopus laevis (African clawed frog)
DOID:0111349
  • hereditary desmoid disease
  • Aliases:
    • FIF
    • familial infiltrative fibromatosis
Homo sapiens (human)
DOID:13269
  • hereditary coproporphyria
  • Aliases:
    • Coproporphyrinogen oxidase deficiency
    • hereditary coproporphyria porphyria
Mus musculus (house mouse)
DOID:13269
  • hereditary coproporphyria
  • Aliases:
    • Coproporphyrinogen oxidase deficiency
    • hereditary coproporphyria porphyria
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:0050951
  • hereditary ataxia
Drosophila melanogaster (fruit fly)
DOID:0050951
  • hereditary ataxia
Danio rerio (zebrafish)
DOID:0050951
  • hereditary ataxia
Mus musculus (house mouse)
DOID:0050951
  • hereditary ataxia
Saccharomyces cerevisiae S288C
DOID:0050951
  • hereditary ataxia
Rattus norvegicus (Norway rat)
DOID:0050951
  • hereditary ataxia
Homo sapiens (human)
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: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
Rattus norvegicus (Norway rat)
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
Mus musculus (house mouse)
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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