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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 2951 - 2975 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0112113
  • combined oxidative phosphorylation deficiency 45
  • Aliases:
    • COXPD45
Saccharomyces cerevisiae S288C
DOID:0080832
  • mild cognitive impairment
Drosophila melanogaster (fruit fly)
DOID:13258
  • typhoid fever
  • Aliases:
    • Typhoid
Saccharomyces cerevisiae S288C
DOID:0050909
  • extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue
  • Aliases:
    • MALT lymphoma
    • MALT lymphoma of the dura
    • mucosa-associated lymphoid tissue lymphoma
Homo sapiens (human)
DOID:10159
  • osteonecrosis
  • Aliases:
    • Avascular necrosis of bone
    • aseptic necrosis
    • bone necrosis
Saccharomyces cerevisiae S288C
DOID:0070111
  • Niemann-Pick disease type A
Caenorhabditis elegans
DOID:9955
  • hypoplastic left heart syndrome
Homo sapiens (human)
DOID:1596
  • depressive disorder
  • Aliases:
    • mental depression
Xenopus laevis (African clawed frog)
DOID:10608
  • celiac disease
  • Aliases:
    • celiac sprue
    • coeliac disease
    • idiopathic steatorrhea
Mus musculus (house mouse)
DOID:0080736
  • Ehlers-Danlos syndrome musculocontractural type 1
Xenopus tropicalis (tropical clawed frog)
DOID:10587
  • Krabbe disease
  • Aliases:
    • Diffuse globoid body sclerosis
    • GLOBOID CELL LEUKOENCEPHALOPATHY
    • Galactosylceramide beta-galactosidase deficiency
    • Krabbe's disease
    • Krabbe's leukodystrophy
    • beta galactocerebrosidase deficiency
    • globoid cell leukodystrophy
Danio rerio (zebrafish)
DOID:10140
  • dry eye syndrome
  • Aliases:
    • Tear film insufficiency
    • dry eye disease
Drosophila melanogaster (fruit fly)
DOID:0050559
  • Fukuyama congenital muscular dystrophy
Homo sapiens (human)
DOID:636
  • central pontine myelinolysis
  • Aliases:
    • osmotic demyelination syndrome
Rattus norvegicus (Norway rat)
DOID:2224
  • essential thrombocythemia
  • Aliases:
    • Essential thrombocythaemia
    • familial thrombocytosis
    • hemorrhagic thrombocythemia
    • hereditary thrombocythemia
    • primary Thrombocytosis
Mus musculus (house mouse)
DOID:0110633
  • rigid spine muscular dystrophy 1
  • Aliases:
    • Eichsfeld type congenital muscular dystrophy
    • MDRS1
    • RSMD1
    • RSS
    • SEPN1-related myopathy
    • classic MmD
    • classic multiminicore disease
    • classic multiminicore myopathy
    • congenital merosin-positive muscular dystrophy with early spine rigidity
    • desmin-related myopathy with Mallory bodies
    • desmin-related myopathy with Mallory body-like inclusions
    • early-onset desmin-related myopathy
    • rigid spine syndrome
    • severe classic form minicore myopathy
    • severe classic form multicore myopathy
    • severe classic form multiminicore disease
Xenopus tropicalis (tropical clawed frog)
DOID:0050831
  • familial encephalopathy with neuroserpin inclusion bodies
  • Aliases:
    • FENIB
Caenorhabditis elegans
DOID:2450
  • central retinal vein occlusion
Rattus norvegicus (Norway rat)
DOID:0070168
  • spermatogenic failure 3
  • Aliases:
    • SPGF3
Mus musculus (house mouse)
DOID:11724
  • limb-girdle muscular dystrophy
  • Aliases:
    • Erb's muscular dystrophy
    • Leyden-Mbius muscular dystrophy
    • limb girdle muscular dystrophy
Saccharomyces cerevisiae S288C
DOID:0060832
  • Griscelli syndrome type 1
  • Aliases:
    • GS1
    • Griscelli syndrome with neurological impairment
    • Griscelli syndrome, cutaneous and neurological type
    • Griscelli-Prunieras syndrome type 1
    • hypopigmentation-neurologic impairment syndrome
Homo sapiens (human)
DOID:1070
  • primary open angle glaucoma
  • Aliases:
    • chronic simple glaucoma
Danio rerio (zebrafish)
DOID:0080431
  • developmental and epileptic encephalopathy 19
  • Aliases:
    • DEE19
    • early infantile epileptic encephalopathy 19
Mus musculus (house mouse)
DOID:0080491
  • cerebral cavernous malformation 1
Homo sapiens (human)
DOID:653
  • purine-pyrimidine metabolic disorder
  • Aliases:
    • inborn errors of purine-pyrimidine metabolism
Homo sapiens (human)
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Last updated: December 9, 2024