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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 4676 - 4700 of 15957 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:0070417
  • neurodevelopmental disorder with speech impairment and dysmorphic facies
  • Aliases:
    • NEDSID
Mus musculus (house mouse)
DOID:0070059
  • autosomal dominant intellectual developmental disorder 29
  • Aliases:
    • MRD29
    • autosomal dominant mental retardation 29
    • autosomal dominant non-syndromic intellectual disability 29
Mus musculus (house mouse)
DOID:0070509
  • Schinzel Giedion syndrome
  • Aliases:
    • SGS
    • Schinzel-Giedion midface retraction syndrome
Mus musculus (house mouse)
DOID:0110346
  • osteogenesis imperfecta type 10
  • Aliases:
    • OI10
    • osteogenesis imperfecta type X
Rattus norvegicus (Norway rat)
DOID:0111144
  • preterm premature rupture of the membranes
  • Aliases:
    • PPROM
Rattus norvegicus (Norway rat)
DOID:0110346
  • osteogenesis imperfecta type 10
  • Aliases:
    • OI10
    • osteogenesis imperfecta type X
Mus musculus (house mouse)
DOID:0080939
  • hereditary angioedema type I
Rattus norvegicus (Norway rat)
DOID:0080939
  • hereditary angioedema type I
Mus musculus (house mouse)
DOID:0060601
  • alpha-2-plasmin inhibitor deficiency
  • Aliases:
    • antiplasmin defiency
    • plasmin inhibitor deficiency
Mus musculus (house mouse)
DOID:0110350
  • osteogenesis imperfecta type 6
  • Aliases:
    • OI6
    • osteogenesis imperfecta type VI
Mus musculus (house mouse)
DOID:13514
  • venous tributary occlusion of retina
  • Aliases:
    • Venous tributary (branch) occlusion of retina
    • Venous tributary branch occlusion of retina
Mus musculus (house mouse)
DOID:0111046
  • platelet-type bleeding disorder 10
  • Aliases:
    • BDPLT10
    • CD36 deficiency
    • platelet glycoprotein IV deficiency
Rattus norvegicus (Norway rat)
DOID:74
  • hematopoietic system disease
  • Aliases:
    • Blood disease
    • Blood dyscrasia
    • DISEASE OF THE BLOOD AND BLOOD-FORMING ORGANS
    • Hematological disease
    • blood disorder
    • disease of haematopoietic system
    • disease of hematopoietic system
    • haematopoietic system disease
Rattus norvegicus (Norway rat)
DOID:0060181
  • ischemic colitis
Rattus norvegicus (Norway rat)
DOID:0050831
  • familial encephalopathy with neuroserpin inclusion bodies
  • Aliases:
    • FENIB
Rattus norvegicus (Norway rat)
DOID:0050117
  • disease by infectious agent
  • Aliases:
    • infectious disease
Rattus norvegicus (Norway rat)
DOID:0111901
  • heparin cofactor II deficiency
  • Aliases:
    • HCF 2 deficiency
    • HCF II deficiency
    • THPH10
    • thrombophilia due to heparin cofactor II deficiency
Rattus norvegicus (Norway rat)
DOID:0111901
  • heparin cofactor II deficiency
  • Aliases:
    • HCF 2 deficiency
    • HCF II deficiency
    • THPH10
    • thrombophilia due to heparin cofactor II deficiency
Mus musculus (house mouse)
DOID:3755
  • antithrombin III deficiency
  • Aliases:
    • AT III deficiency
    • hereditary thrombophilia due to congenital antithrombin deficiency
Mus musculus (house mouse)
DOID:0090030
  • corticosteroid-binding globulin deficiency
  • Aliases:
    • CBG deficiency
    • transcortin deficiency
Rattus norvegicus (Norway rat)
DOID:0090030
  • corticosteroid-binding globulin deficiency
  • Aliases:
    • CBG deficiency
    • transcortin deficiency
Mus musculus (house mouse)
DOID:0050831
  • familial encephalopathy with neuroserpin inclusion bodies
  • Aliases:
    • FENIB
Mus musculus (house mouse)
DOID:0060186
  • chemical colitis
Mus musculus (house mouse)
DOID:13372
  • alpha 1-antitrypsin deficiency
  • Aliases:
    • AAT deficiency
Mus musculus (house mouse)
DOID:0060186
  • chemical colitis
Rattus norvegicus (Norway rat)
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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