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 15351 - 15375 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0050827
  • rheumatic heart disease
  • Aliases:
    • rheumatic carditis
Saccharomyces cerevisiae S288C
DOID:14400
  • capillary leak syndrome
Homo sapiens (human)
DOID:0080745
  • polymyositis
Drosophila melanogaster (fruit fly)
DOID:0110463
  • autosomal recessive nonsyndromic deafness 102
  • Aliases:
    • DFNB102
    • autosomal recessive deafness 102
Mus musculus (house mouse)
DOID:0060684
  • autosomal dominant nocturnal frontal lobe epilepsy 3
  • Aliases:
    • ENFL3
    • nocturnal frontal lobe epilepsy 3
Mus musculus (house mouse)
DOID:0050633
  • ocular albinism 1
  • Aliases:
    • Albinism ocular 1
    • ocular albinism
Caenorhabditis elegans
DOID:0060366
  • Hennekam syndrome
  • Aliases:
    • Hennekam lymphangiectasia-lymphedema syndrome
    • lymphedem-lymphangiectasia-intellectual disability syndrome
Mus musculus (house mouse)
DOID:0050968
  • autosomal dominant cerebellar ataxia, deafness and narcolepsy
Mus musculus (house mouse)
DOID:11724
  • limb-girdle muscular dystrophy
  • Aliases:
    • Erb's muscular dystrophy
    • Leyden-Mbius muscular dystrophy
    • limb girdle muscular dystrophy
Rattus norvegicus (Norway rat)
DOID:0081220
  • autosomal recessive intellectual developmental disorder 58
Homo sapiens (human)
DOID:4972
  • myelodysplastic/myeloproliferative neoplasm
  • Aliases:
    • Myeloproliferative/Myelodysplastic syndromes
    • myelodysplastic myeloproliferative cancer
Homo sapiens (human)
DOID:0111691
  • familial adult myoclonic epilepsy 5
  • Aliases:
    • FAME5
    • FCMTE5
    • familial cortical myoclonic tremor and epilepsy 5
Mus musculus (house mouse)
DOID:11165
  • common wart
Mus musculus (house mouse)
DOID:0111498
  • combined oxidative phosphorylation deficiency 22
  • Aliases:
    • COXPD22
Homo sapiens (human)
DOID:0111162
  • epidermal nevus
  • Aliases:
    • nonepidermolytic keratinocytic nevus
Rattus norvegicus (Norway rat)
DOID:0050753
  • cerebellar ataxia
Homo sapiens (human)
DOID:0050425
  • restless legs syndrome
  • Aliases:
    • WED
    • Willis-Ekbom disease
    • Wittmaack-Ekbom syndrome
Drosophila melanogaster (fruit fly)
DOID:0110435
  • dilated cardiomyopathy 1GG
  • Aliases:
    • CMD1GG
Homo sapiens (human)
DOID:2596
  • larynx cancer
Rattus norvegicus (Norway rat)
DOID:0090134
  • complex cortical dysplasia with other brain malformations 3
  • Aliases:
    • CDCBM3
Mus musculus (house mouse)
DOID:2018
  • hyperinsulinism
  • Aliases:
    • hyperinsulinemia
Rattus norvegicus (Norway rat)
DOID:0111605
  • distal arthrogryposis type 2A
  • Aliases:
    • DA2A
    • distal arthrogryposis type 2A (Freeman-Sheldon)
Homo sapiens (human)
DOID:11724
  • limb-girdle muscular dystrophy
  • Aliases:
    • Erb's muscular dystrophy
    • Leyden-Mbius muscular dystrophy
    • limb girdle muscular dystrophy
Drosophila melanogaster (fruit fly)
DOID:13994
  • cleidocranial dysplasia
  • Aliases:
    • Marie-Sainton Disease
    • cleidocranial dysostosis
Mus musculus (house mouse)
DOID:0070199
  • Miyoshi muscular dystrophy 1
  • Aliases:
    • MMD1
    • Miyoshi myopathy 1
Mus musculus (house mouse)

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 9, 2024