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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 11501 - 11525 of 15957 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism Source
DOID:0080734
  • Ehlers-Danlos syndrome kyphoscoliotic type 1
Mus musculus (house mouse)
DOID:0080733
  • Ehlers-Danlos syndrome dermatosparaxis type
Homo sapiens (human)
DOID:0080733
  • Ehlers-Danlos syndrome dermatosparaxis type
Mus musculus (house mouse)
DOID:0080732
  • Ehlers-Danlos syndrome classic-like 2
Homo sapiens (human)
DOID:0080732
  • Ehlers-Danlos syndrome classic-like 2
Mus musculus (house mouse)
DOID:0080732
  • Ehlers-Danlos syndrome classic-like 2
Rattus norvegicus (Norway rat)
DOID:0080730
  • Ehlers-Danlos syndrome cardiac valvular type
Rattus norvegicus (Norway rat)
DOID:0080730
  • Ehlers-Danlos syndrome cardiac valvular type
Mus musculus (house mouse)
DOID:0080730
  • Ehlers-Danlos syndrome cardiac valvular type
Homo sapiens (human)
DOID:0080728
  • Ehlers-Danlos syndrome arthrochalasia type 2
Mus musculus (house mouse)
DOID:0080728
  • Ehlers-Danlos syndrome arthrochalasia type 2
Rattus norvegicus (Norway rat)
DOID:0080728
  • Ehlers-Danlos syndrome arthrochalasia type 2
Homo sapiens (human)
DOID:0080727
  • Ehlers-Danlos syndrome arthrochalasia type 1
Homo sapiens (human)
DOID:0080727
  • Ehlers-Danlos syndrome arthrochalasia type 1
Mus musculus (house mouse)
DOID:0080727
  • Ehlers-Danlos syndrome arthrochalasia type 1
Rattus norvegicus (Norway rat)
DOID:0080726
  • Ehlers-Danlos syndrome classic type 2
Homo sapiens (human)
DOID:0080726
  • Ehlers-Danlos syndrome classic type 2
Mus musculus (house mouse)
DOID:0080722
  • Kenny-Caffey syndrome type 1
Saccharomyces cerevisiae S288C
DOID:0080722
  • Kenny-Caffey syndrome type 1
Homo sapiens (human)
DOID:0080721
  • calvarial doughnut lesions with bone fragility
Homo sapiens (human)
DOID:0080720
  • autosomal dominant congenital deafness with onychodystrophy
Mus musculus (house mouse)
DOID:0080719
  • congenital myopathy 6
  • Aliases:
    • inclusion body myopathy 3
    • proximal myopathy and ophthalmoplegia
Mus musculus (house mouse)
DOID:0080719
  • congenital myopathy 6
  • Aliases:
    • inclusion body myopathy 3
    • proximal myopathy and ophthalmoplegia
Homo sapiens (human)
DOID:0080718
  • GNE myopathy
  • Aliases:
    • Distal myopathy, Nonaka type
    • Hereditary Inclusion Body Myopathy
    • Nonaka myopathy
    • inclusion body myopathy 2
Homo sapiens (human)
DOID:0080718
  • GNE myopathy
  • Aliases:
    • Distal myopathy, Nonaka type
    • Hereditary Inclusion Body Myopathy
    • Nonaka myopathy
    • inclusion body myopathy 2
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