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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 4651 - 4675 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▲
DOID:0080981
  • arthrogryposis multiplex congenita-5
Drosophila melanogaster (fruit fly)
DOID:0080981
  • arthrogryposis multiplex congenita-5
Rattus norvegicus (Norway rat)
DOID:0080982
  • X-linked mental retardation-hypotonic facies syndrome-1
Homo sapiens (human)
DOID:0080982
  • X-linked mental retardation-hypotonic facies syndrome-1
Mus musculus (house mouse)
DOID:0080984
  • X-linked intellectual developmental disorder 109
  • Aliases:
    • Fragile XE syndrome
    • fragile site on chromosome Xq28
Drosophila melanogaster (fruit fly)
DOID:0080984
  • X-linked intellectual developmental disorder 109
  • Aliases:
    • Fragile XE syndrome
    • fragile site on chromosome Xq28
Homo sapiens (human)
DOID:0080985
  • syndromic X-linked intellectual disorder Lujan-Fryns-type
Saccharomyces cerevisiae S288C
DOID:0080985
  • syndromic X-linked intellectual disorder Lujan-Fryns-type
Homo sapiens (human)
DOID:0080986
  • Ehlers-Danlos syndrome periodontal type 1
Homo sapiens (human)
DOID:0080986
  • Ehlers-Danlos syndrome periodontal type 1
Mus musculus (house mouse)
DOID:0080987
  • Ehlers-Danlos syndrome periodontal type 2
Homo sapiens (human)
DOID:0080987
  • Ehlers-Danlos syndrome periodontal type 2
Rattus norvegicus (Norway rat)
DOID:0080987
  • Ehlers-Danlos syndrome periodontal type 2
Mus musculus (house mouse)
DOID:0080988
  • pretibial dystrophic epidermolysis bullosa
Mus musculus (house mouse)
DOID:0080988
  • pretibial dystrophic epidermolysis bullosa
Homo sapiens (human)
DOID:0080990
  • King Denborough syndrome
Homo sapiens (human)
DOID:0080990
  • King Denborough syndrome
Mus musculus (house mouse)
DOID:0080991
  • congenital myopathy 1B
  • Aliases:
    • multiminicore disease
Homo sapiens (human)
DOID:0080991
  • congenital myopathy 1B
  • Aliases:
    • multiminicore disease
Mus musculus (house mouse)
DOID:0080998
  • acute necrotizing pancreatitis
Caenorhabditis elegans
DOID:0080998
  • acute necrotizing pancreatitis
Homo sapiens (human)
DOID:0080998
  • acute necrotizing pancreatitis
Rattus norvegicus (Norway rat)
DOID:0080998
  • acute necrotizing pancreatitis
Mus musculus (house mouse)
DOID:0080998
  • acute necrotizing pancreatitis
Drosophila melanogaster (fruit fly)
DOID:0081001
  • Cowden syndrome 5
Mus musculus (house mouse)
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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: December 9, 2024