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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 13651 - 13675 of 15957 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism Source
DOID:0050460
  • Wolf-Hirschhorn syndrome
  • Aliases:
    • 4p deletion syndrome
    • PITT SYNDROME
    • Pitt-Rogers-Danks Syndrome
    • chromosome 4p16.3 deletion syndrome
Rattus norvegicus (Norway rat)
DOID:0050460
  • Wolf-Hirschhorn syndrome
  • Aliases:
    • 4p deletion syndrome
    • PITT SYNDROME
    • Pitt-Rogers-Danks Syndrome
    • chromosome 4p16.3 deletion syndrome
Mus musculus (house mouse)
DOID:0090060
  • Wolcott-Rallison syndrome
Homo sapiens (human)
DOID:0090060
  • Wolcott-Rallison syndrome
Caenorhabditis elegans
DOID:0090060
  • Wolcott-Rallison syndrome
Rattus norvegicus (Norway rat)
DOID:0090060
  • Wolcott-Rallison syndrome
Drosophila melanogaster (fruit fly)
DOID:0090060
  • Wolcott-Rallison syndrome
Mus musculus (house mouse)
DOID:9169
  • Wiskott-Aldrich syndrome
  • Aliases:
    • Wiskott syndrome
Saccharomyces cerevisiae S288C
DOID:9169
  • Wiskott-Aldrich syndrome
  • Aliases:
    • Wiskott syndrome
Mus musculus (house mouse)
DOID:9169
  • Wiskott-Aldrich syndrome
  • Aliases:
    • Wiskott syndrome
Homo sapiens (human)
DOID:0080696
  • Winchester syndrome
Homo sapiens (human)
DOID:0060814
  • Wilson-Turner syndrome
  • Aliases:
    • MRXS6
    • WTS
    • X-linked intellectual disability-gynecomastia-obesity syndrome
    • mental retardation, X-linked, syndromic 6
    • mental retardation, X-linked, with gynecomastia and obesity
Mus musculus (house mouse)
DOID:0060814
  • Wilson-Turner syndrome
  • Aliases:
    • MRXS6
    • WTS
    • X-linked intellectual disability-gynecomastia-obesity syndrome
    • mental retardation, X-linked, syndromic 6
    • mental retardation, X-linked, with gynecomastia and obesity
Homo sapiens (human)
DOID:893
  • Wilson disease
  • Aliases:
    • Cerebral pseudosclerosis
    • Westphal pseudosclerosis
    • Westphal-Strumpell syndrome
    • Wilson's disease
    • hepatolenticular degeneration
Drosophila melanogaster (fruit fly)
DOID:893
  • Wilson disease
  • Aliases:
    • Cerebral pseudosclerosis
    • Westphal pseudosclerosis
    • Westphal-Strumpell syndrome
    • Wilson's disease
    • hepatolenticular degeneration
Mus musculus (house mouse)
DOID:893
  • Wilson disease
  • Aliases:
    • Cerebral pseudosclerosis
    • Westphal pseudosclerosis
    • Westphal-Strumpell syndrome
    • Wilson's disease
    • hepatolenticular degeneration
Rattus norvegicus (Norway rat)
DOID:893
  • Wilson disease
  • Aliases:
    • Cerebral pseudosclerosis
    • Westphal pseudosclerosis
    • Westphal-Strumpell syndrome
    • Wilson's disease
    • hepatolenticular degeneration
Saccharomyces cerevisiae S288C
DOID:893
  • Wilson disease
  • Aliases:
    • Cerebral pseudosclerosis
    • Westphal pseudosclerosis
    • Westphal-Strumpell syndrome
    • Wilson's disease
    • hepatolenticular degeneration
Caenorhabditis elegans
DOID:893
  • Wilson disease
  • Aliases:
    • Cerebral pseudosclerosis
    • Westphal pseudosclerosis
    • Westphal-Strumpell syndrome
    • Wilson's disease
    • hepatolenticular degeneration
Homo sapiens (human)
DOID:1928
  • Williams-Beuren syndrome
  • Aliases:
    • Fanconi Schlesinger syndrome
    • WBS
Caenorhabditis elegans
DOID:1928
  • Williams-Beuren syndrome
  • Aliases:
    • Fanconi Schlesinger syndrome
    • WBS
Mus musculus (house mouse)
DOID:1928
  • Williams-Beuren syndrome
  • Aliases:
    • Fanconi Schlesinger syndrome
    • WBS
Xenopus laevis (African clawed frog)
DOID:1928
  • Williams-Beuren syndrome
  • Aliases:
    • Fanconi Schlesinger syndrome
    • WBS
Homo sapiens (human)
DOID:0081333
  • Wiedemann-Rautenstrauch syndrome
  • Aliases:
    • Neonatal progeroid syndrome
    • PROGEROID SYNDROME, NEONATAL
Homo sapiens (human)
DOID:0070067
  • White-Sutton syndrome
  • Aliases:
    • MRD37
    • WHSUS
    • autosomal dominant mental retardation 37
Mus musculus (house mouse)
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Last updated: December 9, 2024