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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 7176 - 7200 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:0060231
  • Bruck syndrome
  • Aliases:
    • osteogenesis imperfecta with congenital joint contractures
Mus musculus (house mouse)
DOID:0080622
  • peroxisome biogenesis disorder 2B
Mus musculus (house mouse)
DOID:2602
  • chondroma
  • Aliases:
    • central Chondroma
Mus musculus (house mouse)
DOID:0070117
  • Meckel syndrome 3
  • Aliases:
    • MKS3
    • Meckel-Gruber syndrome, type 3
Mus musculus (house mouse)
DOID:0080931
  • primary localized cutaneous amyloidosis 2
Mus musculus (house mouse)
DOID:3324
  • mood disorder
  • Aliases:
    • episodic mood disorder
Mus musculus (house mouse)
DOID:0110540
  • autosomal recessive nonsyndromic deafness 98
  • Aliases:
    • DFNB98
    • autosomal recessive deafness 98
Mus musculus (house mouse)
DOID:0110055
  • amelogenesis imperfecta type 3A
  • Aliases:
    • ADHCAI
    • amelogenesis imperfecta hypomineralization type
    • amelogenesis imperfecta type III
    • autosomal dominant amelogenesis imperfecta hypocalcification type
Mus musculus (house mouse)
DOID:0110509
  • autosomal recessive nonsyndromic deafness 53
  • Aliases:
    • DFNB53
    • autosomal recessive deafness 53
Mus musculus (house mouse)
DOID:9253
  • gastrointestinal stromal tumor
  • Aliases:
    • GANT
    • GIST
    • Stromal tumor of gastrointestinal tract
    • Stromal tumour of gastrointestinal tract
    • gastrointestinal stromal tumour
Mus musculus (house mouse)
DOID:0112035
  • non-syndromic X-linked intellectual disability 96
  • Aliases:
    • MRX96
    • X-linked mental retardation 96
Mus musculus (house mouse)
DOID:14679
  • VACTERL association
Mus musculus (house mouse)
DOID:0090017
  • epidermolysis bullosa simplex with muscular dystrophy
  • Aliases:
    • epidermolysis bullosa simplex and limb-girdle muscular dystrophy
    • limb-girdle muscular dystrophy with epidermolysis bullosa simplex
Mus musculus (house mouse)
DOID:0080294
  • Charcot-Marie-Tooth disease dominant intermediate G
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:0070469
  • neurodevelopmental disorder with dysmorphic facies and thin corpus callosum
  • Aliases:
    • NEDDFAC
Mus musculus (house mouse)
DOID:9521
  • Laron syndrome
  • Aliases:
    • Laron-type isolated somatotropin defect
Mus musculus (house mouse)
DOID:3275
  • thymoma
Mus musculus (house mouse)
DOID:5688
  • Werner syndrome
  • Aliases:
    • WS
    • Werner's syndrome
    • adult premature ageing syndrome
    • adult progeria
Mus musculus (house mouse)
DOID:0111272
  • occipital horn syndrome
  • Aliases:
    • EDS IX
    • Ehlers-Danlos syndrome type 9
    • Ehlers-Danlos syndrome type IX
    • X-linked cutis laxa
Mus musculus (house mouse)
DOID:0070270
  • hereditary nonpolyposis colorectal cancer type 8
  • Aliases:
    • HNPCC8
Mus musculus (house mouse)
DOID:0070287
  • primary autosomal recessive microcephaly 11
  • Aliases:
    • MCPH11
Mus musculus (house mouse)
DOID:0050127
  • sinusitis
Mus musculus (house mouse)
DOID:0080325
  • tuberous sclerosis 2
Mus musculus (house mouse)
DOID:0080461
  • developmental and epileptic encephalopathy 26
  • Aliases:
    • DEE26
    • early infantile epileptic encephalopathy 26
Mus musculus (house mouse)
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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