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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 4601 - 4625 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▲
DOID:0080940
  • hereditary angioedema type III
Mus musculus (house mouse)
DOID:0080941
  • acquired angioedema
Rattus norvegicus (Norway rat)
DOID:0080941
  • acquired angioedema
Homo sapiens (human)
DOID:0080941
  • acquired angioedema
Mus musculus (house mouse)
DOID:0080943
  • 46,XX sex reversal 5
Homo sapiens (human)
DOID:0080943
  • 46,XX sex reversal 5
Mus musculus (house mouse)
DOID:0080944
  • familial Behcet-like autoinflammatory syndrome
  • Aliases:
    • A20 haploinsufficiency
Homo sapiens (human)
DOID:0080944
  • familial Behcet-like autoinflammatory syndrome
  • Aliases:
    • A20 haploinsufficiency
Mus musculus (house mouse)
DOID:0080946
  • retinal dystrophy with leukodystrophy
  • Aliases:
    • ACBD5 deficiency
Mus musculus (house mouse)
DOID:0080946
  • retinal dystrophy with leukodystrophy
  • Aliases:
    • ACBD5 deficiency
Homo sapiens (human)
DOID:0080948
  • agenesis of corpus callosum, cardiac, ocular, and genital syndrome
Mus musculus (house mouse)
DOID:0080948
  • agenesis of corpus callosum, cardiac, ocular, and genital syndrome
Homo sapiens (human)
DOID:0080948
  • agenesis of corpus callosum, cardiac, ocular, and genital syndrome
Rattus norvegicus (Norway rat)
DOID:0080948
  • agenesis of corpus callosum, cardiac, ocular, and genital syndrome
Danio rerio (zebrafish)
DOID:0080948
  • agenesis of corpus callosum, cardiac, ocular, and genital syndrome
Xenopus laevis (African clawed frog)
DOID:0080950
  • alopecia-mental retardation syndrome 4
Homo sapiens (human)
DOID:0080952
  • AMED syndrome
  • Aliases:
    • AMEDS
Homo sapiens (human)
DOID:0080953
  • amelogenesis imperfecta type 1J
  • Aliases:
    • Amelogenesis imperfecta, type IJ
Caenorhabditis elegans
DOID:0080953
  • amelogenesis imperfecta type 1J
  • Aliases:
    • Amelogenesis imperfecta, type IJ
Xenopus laevis (African clawed frog)
DOID:0080953
  • amelogenesis imperfecta type 1J
  • Aliases:
    • Amelogenesis imperfecta, type IJ
Homo sapiens (human)
DOID:0080954
  • arthrogryposis multiplex congenita
Drosophila melanogaster (fruit fly)
DOID:0080954
  • arthrogryposis multiplex congenita
Mus musculus (house mouse)
DOID:0080954
  • arthrogryposis multiplex congenita
Homo sapiens (human)
DOID:0080957
  • primary hypoalphalipoproteinemia 1
  • Aliases:
    • familial HDL deficiency
    • familial hypoalphalipoproteinemia
Mus musculus (house mouse)
DOID:0080957
  • primary hypoalphalipoproteinemia 1
  • Aliases:
    • familial HDL deficiency
    • familial hypoalphalipoproteinemia
Caenorhabditis elegans
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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