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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 January 28, 2025
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 901 - 925 of 5716 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism Source
DOID:0060895
  • Parkinson's disease 4
  • Aliases:
    • autosomal dominant Lewy body Parkinson disease 4
    • autosomal dominant Parkinson disease 4
    • autosomal dominant Parkinson's disease 4
Homo sapiens (human)
DOID:0060895
  • Parkinson's disease 4
  • Aliases:
    • autosomal dominant Lewy body Parkinson disease 4
    • autosomal dominant Parkinson disease 4
    • autosomal dominant Parkinson's disease 4
Mus musculus (house mouse)
DOID:0060896
  • Parkinson's disease 23
  • Aliases:
    • autosomal recessive early-onset Parkinson disease 23
    • autosomal recessive early-onset Parkinson's disease 23
Homo sapiens (human)
DOID:0060898
  • Parkinson's disease 20
  • Aliases:
    • early-onset Parkinson disease 20
    • early-onset Parkinson's disease 20
Homo sapiens (human)
DOID:0060900
  • Parkinson's disease 14
  • Aliases:
    • Dystonia-Parkinsonism Adult-Onset
    • autosomal recessive Parkinson disease 14
    • autosomal recessive Parkinson's disease 14
Homo sapiens (human)
DOID:0060900
  • Parkinson's disease 14
  • Aliases:
    • Dystonia-Parkinsonism Adult-Onset
    • autosomal recessive Parkinson disease 14
    • autosomal recessive Parkinson's disease 14
Mus musculus (house mouse)
DOID:0060901
  • lymphoplasmacytic lymphoma
  • Aliases:
    • Waldenstroem's macroglobulinemia
    • Waldenstrom Macroglobulinemia
    • lymphoplasmacytic lymphoma with IgM gammopathy
Homo sapiens (human)
DOID:0060902
  • Norman-Roberts syndrome
  • Aliases:
    • lissencephaly 2
    • lissencephaly syndrome, Norman-Roberts type
Homo sapiens (human)
DOID:0060903
  • thrombosis
Rattus norvegicus (Norway rat)
DOID:0060903
  • thrombosis
Homo sapiens (human)
DOID:0060912
  • craniosynostosis 7
  • Aliases:
    • CRS7
Homo sapiens (human)
DOID:0060916
  • proteasome-associated autoinflammatory syndrome 3
  • Aliases:
    • PRAAS3
Homo sapiens (human)
DOID:0060917
  • facioscapulohumeral muscular dystrophy 3
  • Aliases:
    • FSHD3
    • facioscapulohumeral muscular dystrophy type 3
Homo sapiens (human)
DOID:0060929
  • non-syndromic X-linked intellectual developmental disorder 111
  • Aliases:
    • XLID111
Homo sapiens (human)
DOID:0060929
  • non-syndromic X-linked intellectual developmental disorder 111
  • Aliases:
    • XLID111
Mus musculus (house mouse)
DOID:0060931
  • developmental dysplasia of the hip 1
  • Aliases:
    • DDH1
Homo sapiens (human)
DOID:0060933
  • developmental delay, dysmorphic facies, and brain anomalies
  • Aliases:
    • DEVDFB
Homo sapiens (human)
DOID:0060936
  • dystonia 28, childhood-onset
  • Aliases:
    • DYSTONIA 28, CHILDHOOD-ONSET
    • DYT28
Homo sapiens (human)
DOID:0060937
  • dystonia 30
  • Aliases:
    • DYT30
Homo sapiens (human)
DOID:0060939
  • dystonia 32
  • Aliases:
    • DYT32
Homo sapiens (human)
DOID:0060940
  • dystonia 33
Homo sapiens (human)
DOID:0060941
  • interstitial lung disease 1
  • Aliases:
    • Idiopathic pulmonary fibrosis
Homo sapiens (human)
DOID:0060942
  • Ullrich congenital muscular dystrophy 1B
Homo sapiens (human)
DOID:0060943
  • Ullrich congenital muscular dystrophy 1C
Homo sapiens (human)
DOID:0060944
  • episodic kinesigenic dyskinesia 3
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 8, 2025