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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 1001 - 1025 of 7942 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism Source
DOID:14515
  • WAGR syndrome
  • Aliases:
    • 11p partial monosomy syndrome
    • Wilms tumor-Aniridia-Genitourinary Anomalies-Mental Retardation syndrome
    • chromosome 11p13 deletion syndrome
Homo sapiens (human)
DOID:0110948
  • Waardenburg syndrome type 1
  • Aliases:
    • WS1
    • Waardenburg syndrome type I
Homo sapiens (human)
DOID:0110949
  • Waardenburg syndrome type 3
  • Aliases:
    • Klein-Waardenburg syndrome
    • WS3
    • Waardenburg syndrome type III
    • Waardenburg syndrome with upper limb anomalies
Homo sapiens (human)
DOID:9258
  • Waardenburg syndrome
  • Aliases:
    • Waardenburg Shah syndrome
    • Waardenburg's syndrome
    • van der Hoeve Halbertsona Waardenburg syndrome
Homo sapiens (human)
DOID:0050560
  • Walker-Warburg syndrome
  • Aliases:
    • HARD syndrome
    • cerebroocular dysplasia-muscular dystrophy syndrome
Saccharomyces cerevisiae S288C
DOID:0050560
  • Walker-Warburg syndrome
  • Aliases:
    • HARD syndrome
    • cerebroocular dysplasia-muscular dystrophy syndrome
Xenopus tropicalis (tropical clawed frog)
DOID:0050560
  • Walker-Warburg syndrome
  • Aliases:
    • HARD syndrome
    • cerebroocular dysplasia-muscular dystrophy syndrome
Xenopus laevis (African clawed frog)
DOID:0050560
  • Walker-Warburg syndrome
  • Aliases:
    • HARD syndrome
    • cerebroocular dysplasia-muscular dystrophy syndrome
Drosophila melanogaster (fruit fly)
DOID:0050560
  • Walker-Warburg syndrome
  • Aliases:
    • HARD syndrome
    • cerebroocular dysplasia-muscular dystrophy syndrome
Homo sapiens (human)
DOID:0050560
  • Walker-Warburg syndrome
  • Aliases:
    • HARD syndrome
    • cerebroocular dysplasia-muscular dystrophy syndrome
Rattus norvegicus (Norway rat)
DOID:0050560
  • Walker-Warburg syndrome
  • Aliases:
    • HARD syndrome
    • cerebroocular dysplasia-muscular dystrophy syndrome
Mus musculus (house mouse)
DOID:0050560
  • Walker-Warburg syndrome
  • Aliases:
    • HARD syndrome
    • cerebroocular dysplasia-muscular dystrophy syndrome
Danio rerio (zebrafish)
DOID:0050560
  • Walker-Warburg syndrome
  • Aliases:
    • HARD syndrome
    • cerebroocular dysplasia-muscular dystrophy syndrome
Caenorhabditis elegans
DOID:0110716
  • Warburg micro syndrome 1
  • Aliases:
    • Micro Syndrome 1
    • WARBM1
Homo sapiens (human)
DOID:0110717
  • Warburg micro syndrome 2
  • Aliases:
    • Micro Syndrome 2
    • WARBM2
Homo sapiens (human)
DOID:0110718
  • Warburg micro syndrome 3
  • Aliases:
    • Micro Syndrome 3
    • WARBM3
Homo sapiens (human)
DOID:0110719
  • Warburg micro syndrome 4
  • Aliases:
    • Micro Syndrome 4
    • WARBM4
Homo sapiens (human)
DOID:0060535
  • Warsaw breakage syndrome
  • Aliases:
    • WABS
Homo sapiens (human)
DOID:9931
  • Waterhouse-Friderichsen syndrome
  • Aliases:
    • Meningococcal hemorrhagic adrenalitis
Homo sapiens (human)
DOID:14731
  • Weaver syndrome
  • Aliases:
    • WEAVER-LIKE SYNDROME
    • Weaver-Williams syndrome
Homo sapiens (human)
DOID:0050475
  • Weill-Marchesani syndrome
  • Aliases:
    • GEMSS syndrome
    • Marchesani-Weill Syndrome
    • Mesodermal Dysmorphodystrophy, Congenital
    • Spherophakia Brachymorphia Syndrome
    • congenital mesodermal dystrophy
Homo sapiens (human)
DOID:0050475
  • Weill-Marchesani syndrome
  • Aliases:
    • GEMSS syndrome
    • Marchesani-Weill Syndrome
    • Mesodermal Dysmorphodystrophy, Congenital
    • Spherophakia Brachymorphia Syndrome
    • congenital mesodermal dystrophy
Mus musculus (house mouse)
DOID:0050475
  • Weill-Marchesani syndrome
  • Aliases:
    • GEMSS syndrome
    • Marchesani-Weill Syndrome
    • Mesodermal Dysmorphodystrophy, Congenital
    • Spherophakia Brachymorphia Syndrome
    • congenital mesodermal dystrophy
Rattus norvegicus (Norway rat)
DOID:4258
  • Weissenbacher-Zweymuller syndrome
  • Aliases:
    • Piere-Robin syndrome
    • Pierre Robin Malformation
Homo sapiens (human)
DOID:13137
  • Werdnig-Hoffmann disease
  • Aliases:
    • HMN (Hereditary motor Neuropathy) Proximal type I
    • SMA1
    • Spinal muscular atrophy 1
    • hereditary motor neuropathy proximal type I
    • infantile muscular atrophy
    • progressive muscular atrophy of infancy
Homo sapiens (human)
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Last updated: August 19, 2024