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 5001 - 5025 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:13810
  • familial hypercholesterolemia
  • Aliases:
    • Fredrickson type IIa hyperlipoproteinemia
    • Fredrickson type IIa lipidaemia
    • familial hyperbetalipoproteinaemia
    • familial hypercholesteremia
    • hyperbetalipoproteinemia
    • type II hyperlipidemia
Caenorhabditis elegans
DOID:0060363
  • glycerol kinase deficiency
Caenorhabditis elegans
DOID:1561
  • cognitive disorder
  • Aliases:
    • cognitive disease
Caenorhabditis elegans
DOID:3525
  • middle cerebral artery infarction
Caenorhabditis elegans
DOID:3602
  • toxic encephalopathy
  • Aliases:
    • neurotoxicity
    • neurotoxicity syndrome
Caenorhabditis elegans
DOID:2218
  • blood platelet disease
  • Aliases:
    • Thrombocytopathy
    • platelet disorder
Caenorhabditis elegans
DOID:9778
  • irritable bowel syndrome
  • Aliases:
    • IBD
    • Irritable colon
Caenorhabditis elegans
DOID:12365
  • malaria
  • Aliases:
    • induced malaria
Caenorhabditis elegans
DOID:2975
  • cystic kidney disease
  • Aliases:
    • renal Cyst
Caenorhabditis elegans
DOID:526
  • human immunodeficiency virus infectious disease
  • Aliases:
    • HIV infection
Caenorhabditis elegans
DOID:75
  • lymphatic system disease
  • Aliases:
    • Lymphangiopathy
    • Lymphatic disease
    • disease of lympoid system
    • disorder of lymph node and lymphatics
    • disorder of lymphatic system
    • disorder of lymphoid system
    • lymphatic disorder
    • lympoid system disease
Caenorhabditis elegans
DOID:0080685
  • aortic dissection
Caenorhabditis elegans
DOID:0050564
  • autosomal dominant nonsyndromic deafness
  • Aliases:
    • autosomal dominant deafness
Caenorhabditis elegans
DOID:0081030
  • central conducting lymphatic anomaly
  • Aliases:
    • lymphatic malformation-7
Caenorhabditis elegans
DOID:0110229
  • cataract 6 multiple types
  • Aliases:
    • CTRCT6
Caenorhabditis elegans
DOID:0111745
  • cerebellar ataxia type 43
  • Aliases:
    • SCA43
Mus musculus (house mouse)
DOID:0110160
  • Charcot-Marie-Tooth disease axonal type 2T
  • Aliases:
    • AR-CMT2T
    • CMT2T
    • Charcot-Marie-Tooth neuropathy type 2T
    • autosomal recessive axonal Charcot-Marie-Tooth disease type 2T
Mus musculus (house mouse)
DOID:3211
  • lysosomal storage disease
  • Aliases:
    • disorder of lysosomal enzyme
    • inborn lysosomal enzyme disorder
    • lysosomal storage metabolism disorder
Caenorhabditis elegans
DOID:0080540
  • galactosialidosis
Caenorhabditis elegans
DOID:3070
  • high grade glioma
  • Aliases:
    • Neuroglial tumor
    • glial cell tumor
    • glioma, malignant
    • malignant Neuroglial tumor
    • malignant glioma
Caenorhabditis elegans
DOID:850
  • lung disease
Caenorhabditis elegans
DOID:0111691
  • familial adult myoclonic epilepsy 5
  • Aliases:
    • FAME5
    • FCMTE5
    • familial cortical myoclonic tremor and epilepsy 5
Caenorhabditis elegans
DOID:0080101
  • Compton-North congenital myopathy
  • Aliases:
    • congenital myopathy 12
Caenorhabditis elegans
DOID:0080030
  • spondyloepimetaphyseal dysplasia, Missouri type
Mus musculus (house mouse)
DOID:0060072
  • benign neoplasm
Homo sapiens (human)

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Last updated: December 9, 2024