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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 2151 - 2175 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0050949
  • autosomal recessive hypophosphatemic rickets
Mus musculus (house mouse)
DOID:0110079
  • Leber congenital amaurosis 8
  • Aliases:
    • LCA8
Homo sapiens (human)
DOID:1389
  • polyneuropathy
Caenorhabditis elegans
DOID:0111054
  • von Willebrand's disease 3
  • Aliases:
    • VWD type 3
    • VWD3
    • von Willebrand disease type 3
    • von Willebrand disease type III
Mus musculus (house mouse)
DOID:0070027
  • CST3-related cerebral amyloid angiopathy
  • Aliases:
    • Amyloidosis VI
    • Amyloidosis, Cerebroarterial, Icelandic Type
    • Cerebral Hemorrhage, Hereditary, with Amyloidosis, Icelandic Variant
    • HCHWA
    • Hereditary Cerebral Hemorrhage with Amyloidosis, Icelandic Variant
Mus musculus (house mouse)
DOID:0060536
  • mitochondrial complex I deficiency
  • Aliases:
    • isolated NADH-CoQ reductase deficiency
    • isolated NADH-coenzyme Q reductase deficiency
    • isolated NADH-ubiquinone reductase deficiency
    • isolated mitochondrial respiratory chain complex I deficiency
Mus musculus (house mouse)
DOID:3007
  • breast ductal carcinoma
  • Aliases:
    • duct carcinoma
Caenorhabditis elegans
DOID:0111839
  • congenital disorder of glycosylation Icc
  • Aliases:
    • congenital disorder of glycosylation type Icc
Saccharomyces cerevisiae S288C
DOID:150
  • disease of mental health
Homo sapiens (human)
DOID:0080438
  • developmental and epileptic encephalopathy 5
  • Aliases:
    • DEE5
    • early infantile epileptic encephalopathy 5
Homo sapiens (human)
DOID:0112259
  • Leydig cell hypoplasia
  • Aliases:
    • 46,XY DSD due to LH resistance or LHB deficiency
    • 46,XY DSD due to luteinizing hormone resistance or luteinizing hormone beta subunit deficiency
    • 46,XY disorder of sex development due to LH resistance or LHB deficiency
    • 46,XY disorder of sex development due to luteinizing hormone resistance or luteinizing hormone beta subunit deficiency
Mus musculus (house mouse)
DOID:0080546
  • non-alcoholic fatty liver
  • Aliases:
    • NAFL
    • nonalcoholic fatty liver
Drosophila melanogaster (fruit fly)
DOID:0081150
  • common variable immunodeficiency 7
Homo sapiens (human)
DOID:0060256
  • Dowling-Degos disease
  • Aliases:
    • dark dot disease
    • reticular pigment anomaly of flexures
Drosophila melanogaster (fruit fly)
DOID:2527
  • nephrosis
Rattus norvegicus (Norway rat)
DOID:0110019
  • age related macular degeneration 7
  • Aliases:
    • ARMD7
Rattus norvegicus (Norway rat)
DOID:6039
  • uveal melanoma
  • Aliases:
    • melanoma of Uvea
Homo sapiens (human)
DOID:10533
  • viral pneumonia
Homo sapiens (human)
DOID:0080788
  • proximal symphalangism 2
Mus musculus (house mouse)
DOID:9220
  • central sleep apnea
  • Aliases:
    • primary central sleep apnea
Drosophila melanogaster (fruit fly)
DOID:0112281
  • spondyloepiphyseal dysplasia Stanescu type
  • Aliases:
    • SED Stanescu type
    • SEDSTN
Xenopus laevis (African clawed frog)
DOID:0050571
  • congenital disorder of glycosylation type II
Danio rerio (zebrafish)
DOID:0111434
  • optic atrophy 10
  • Aliases:
    • OPA10
    • optic atrophy 10 with or without ataxia, mental retardation, and seizures
Mus musculus (house mouse)
DOID:0080596
  • hyper IgE recurrent infection syndrome 4
Mus musculus (house mouse)
DOID:0050426
  • Stevens-Johnson syndrome
Rattus norvegicus (Norway rat)
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024