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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 401 - 425 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0050679
  • blue cone monochromacy
Xenopus laevis (African clawed frog)
DOID:0050572
  • cone-rod dystrophy
  • Aliases:
    • cone-rod retinal dystrophy
Mus musculus (house mouse)
DOID:0050812
  • spondyloepimetaphyseal dysplasia, Pakistani type
  • Aliases:
    • spondyloepimetaphyseal dysplasia Pakistani type
Homo sapiens (human)
DOID:0040091
  • autoimmune pancreatitis
Homo sapiens (human)
DOID:0070394
  • developmental and epileptic encephalopathy 108
  • Aliases:
    • DEE108
    • early infantile epileptic encephalopathy 108
Mus musculus (house mouse)
DOID:0070149
  • hereditary sensory and autonomic neuropathy type 7
  • Aliases:
    • HSAN7
    • hereditary sensory and autonomic neuropathy type VII
Mus musculus (house mouse)
DOID:0080000
  • muscular disease
Caenorhabditis elegans
DOID:0050458
  • juvenile myelomonocytic leukemia
Rattus norvegicus (Norway rat)
DOID:303
  • substance-related disorder
Homo sapiens (human)
DOID:0050890
  • synucleinopathy
  • Aliases:
    • Synucleinopathies
    • alpha Synucleinopathies
Rattus norvegicus (Norway rat)
DOID:5410
  • pulmonary neuroendocrine tumor
Homo sapiens (human)
DOID:0112029
  • non-syndromic X-linked intellectual disability 50
  • Aliases:
    • MRX50
    • X-linked intellectual developmental disorder 50
    • X-linked mental retardation 50
    • XLID50
Rattus norvegicus (Norway rat)
DOID:0060479
  • Shwachman-Diamond syndrome
  • Aliases:
    • Shwachman syndrome
    • Shwachman-Bodian-Diamond syndrome
    • Shwachman-Diamond type metaphyseal dysplasia
    • pancreatic insufficiency and bone marrow dysfunction
Caenorhabditis elegans
DOID:13533
  • osteopetrosis
  • Aliases:
    • Albers-Schonberg disease
    • marble bone
Mus musculus (house mouse)
DOID:0112184
  • thyroid dyshormonogenesis 5
  • Aliases:
    • TDH5
    • genetic defect in thyroid hormonogenesis 5
Mus musculus (house mouse)
DOID:1485
  • cystic fibrosis
  • Aliases:
    • CF
    • mucoviscidosis
Xenopus laevis (African clawed frog)
DOID:0080922
  • bilateral frontoparietal polymicrogyria
Mus musculus (house mouse)
DOID:0080059
  • autosomal recessive spinocerebellar ataxia 7
  • Aliases:
    • SCAR7
Danio rerio (zebrafish)
DOID:0070474
  • childhood-onset neurodegeneration with brain atrophy
  • Aliases:
    • CONDBA
    • childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder
Homo sapiens (human)
DOID:0080821
  • exercise-induced bronchoconstriction
  • Aliases:
    • exercise-induced asthma
Mus musculus (house mouse)
DOID:0050884
  • triosephosphate isomerase deficiency
  • Aliases:
    • Triose phosphate-isomerase deficiency
Drosophila melanogaster (fruit fly)
DOID:0110639
  • congenital muscular dystrophy due to integrin alpha-7 deficiency
  • Aliases:
    • congenital muscular dystrophy with ITGA7 deficiency
    • congenital muscular dystrophy with integrin alpha-7 deficiency
    • congenital myopathy due to integrin alpha-7 deficiency
Homo sapiens (human)
DOID:0081034
  • glutatione synthetase deficiency with 5-oxoprolinuria
Mus musculus (house mouse)
DOID:824
  • periodontitis
  • Aliases:
    • chronic pericementitis
Mus musculus (house mouse)
DOID:0080505
  • Cornelia de Lange syndrome 1
Homo sapiens (human)
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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