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 13551 - 13575 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:0060937
  • dystonia 30
  • Aliases:
    • DYT30
Homo sapiens (human)
DOID:0060936
  • dystonia 28 childhood-onset
  • Aliases:
    • DYSTONIA 28, CHILDHOOD-ONSET
    • DYT28
Homo sapiens (human)
DOID:0060936
  • dystonia 28 childhood-onset
  • Aliases:
    • DYSTONIA 28, CHILDHOOD-ONSET
    • DYT28
Mus musculus (house mouse)
DOID:0060936
  • dystonia 28 childhood-onset
  • Aliases:
    • DYSTONIA 28, CHILDHOOD-ONSET
    • DYT28
Drosophila melanogaster (fruit fly)
DOID:0060933
  • developmental delay, dysmorphic facies, and brain anomalies
  • Aliases:
    • DEVDFB
Homo sapiens (human)
DOID:0060933
  • developmental delay, dysmorphic facies, and brain anomalies
  • Aliases:
    • DEVDFB
Mus musculus (house mouse)
DOID:0060931
  • developmental dysplasia of the hip 1
  • Aliases:
    • DDH1
Homo sapiens (human)
DOID:0060931
  • developmental dysplasia of the hip 1
  • Aliases:
    • DDH1
Mus musculus (house mouse)
DOID:0060929
  • non-syndromic X-linked intellectual developmental disorder 111
  • Aliases:
    • XLID111
Mus musculus (house mouse)
DOID:0060929
  • non-syndromic X-linked intellectual developmental disorder 111
  • Aliases:
    • XLID111
Homo sapiens (human)
DOID:0060917
  • facioscapulohumeral muscular dystrophy 3
  • Aliases:
    • FSHD3
    • facioscapulohumeral muscular dystrophy type 3
Homo sapiens (human)
DOID:0060917
  • facioscapulohumeral muscular dystrophy 3
  • Aliases:
    • FSHD3
    • facioscapulohumeral muscular dystrophy type 3
Mus musculus (house mouse)
DOID:0060916
  • proteasome-associated autoinflammatory syndrome 3
  • Aliases:
    • PRAAS3
Homo sapiens (human)
DOID:0060912
  • craniosynostosis 7
  • Aliases:
    • CRS7
Homo sapiens (human)
DOID:0060903
  • thrombosis
Rattus norvegicus (Norway rat)
DOID:0060903
  • thrombosis
Caenorhabditis elegans
DOID:0060903
  • thrombosis
Danio rerio (zebrafish)
DOID:0060903
  • thrombosis
Drosophila melanogaster (fruit fly)
DOID:0060903
  • thrombosis
Homo sapiens (human)
DOID:0060903
  • thrombosis
Mus musculus (house mouse)
DOID:0060902
  • Norman-Roberts syndrome
  • Aliases:
    • lissencephaly 2
    • lissencephaly syndrome, Norman-Roberts type
Rattus norvegicus (Norway rat)
DOID:0060902
  • Norman-Roberts syndrome
  • Aliases:
    • lissencephaly 2
    • lissencephaly syndrome, Norman-Roberts type
Mus musculus (house mouse)
DOID:0060902
  • Norman-Roberts syndrome
  • Aliases:
    • lissencephaly 2
    • lissencephaly syndrome, Norman-Roberts type
Homo sapiens (human)
DOID:0060901
  • lymphoplasmacytic lymphoma
  • Aliases:
    • Waldenstroem's macroglobulinemia
    • Waldenstrom Macroglobulinemia
    • lymphoplasmacytic lymphoma with IgM gammopathy
Homo sapiens (human)
DOID:0060901
  • lymphoplasmacytic lymphoma
  • Aliases:
    • Waldenstroem's macroglobulinemia
    • Waldenstrom Macroglobulinemia
    • lymphoplasmacytic lymphoma with IgM gammopathy
Rattus norvegicus (Norway rat)

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 9, 2024