GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 826 - 850 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism
DOID:5679
  • retinal disease
Homo sapiens (human)
DOID:437
  • myasthenia gravis
Homo sapiens (human)
DOID:594
  • panic disorder
  • Aliases:
    • panic anxiety syndrome
Homo sapiens (human)
DOID:9471
  • meningitis
Homo sapiens (human)
DOID:12156
  • arachnoiditis
Homo sapiens (human)
DOID:13001
  • carotid stenosis
  • Aliases:
    • Carotid artery stenosis
    • Stenosis, carotid artery
Homo sapiens (human)
DOID:5614
  • eye disease
Homo sapiens (human)
DOID:0050495
  • exanthema subitum
  • Aliases:
    • Roseola Infantum
    • Sixth Disease
Homo sapiens (human)
DOID:0050508
  • variola major
Homo sapiens (human)
DOID:8729
  • milker's nodule
  • Aliases:
    • Milkers' node
    • Paravaccinia
    • milker nodule
Homo sapiens (human)
DOID:8337
  • appendicitis
  • Aliases:
    • acute appendicitis
    • acute appendicitis with generalized peritonitis
    • acute appendicitis with peritoneal abscess
Homo sapiens (human)
DOID:1270
  • hereditary hemorrhagic telangiectasia
  • Aliases:
    • Osler hemorrhagic telangiectasia syndrome
    • Osler-Weber-Rendu disease
    • Rendu-Osler-Weber disease
Homo sapiens (human)
DOID:1272
  • telangiectasis
  • Aliases:
    • telangiectasia
Homo sapiens (human)
DOID:1271
  • capillary disease
  • Aliases:
    • disease of capillaries
Homo sapiens (human)
DOID:14250
  • Down syndrome
  • Aliases:
    • Complete trisomy 21 syndrome
    • Down's syndrome
    • Down's syndrome - trisomy 21
    • Downs syndrome
    • G Trisomy
    • trisomy 21 syndrome
Homo sapiens (human)
DOID:0050729
  • Chanarin-Dorfman syndrome
  • Aliases:
    • neutral lipid storage disease
Homo sapiens (human)
DOID:9263
  • homocystinuria
  • Aliases:
    • CBS deficiency
    • cystathionine beta synthase deficiency
    • cystathionine synthase deficiency
Homo sapiens (human)
DOID:8456
  • choline deficiency disease
  • Aliases:
    • choline deficiency
Homo sapiens (human)
DOID:3765
  • pseudohermaphroditism
  • Aliases:
    • Indeterminate sex and pseudohermaphroditism
Homo sapiens (human)
DOID:1923
  • disorder of sexual development
  • Aliases:
    • sex development disorder
    • sex differentiation disease
Homo sapiens (human)
DOID:3763
  • hermaphroditism
Homo sapiens (human)
DOID:718
  • autoimmune hemolytic anemia
  • Aliases:
    • Autoimmune haemolytic anaemia
    • autoimmune hemolytic anaemia
Homo sapiens (human)
DOID:14723
  • beta-ketothiolase deficiency
  • Aliases:
    • 2-methyl-3-hydroxybutyricacidemia
    • 3-ketothiolase deficiency
    • 3-oxothiolase deficiency
    • Mitochondrial acetoacetyl-CoA Thiolase deficiency
    • alpha-methylacetoaceticaciduria
    • peroxisomal thiolase deficiency
Homo sapiens (human)
DOID:1340
  • pure red-cell aplasia
  • Aliases:
    • Red cell hypoplasia
    • primary red cell aplasia
    • pure red cell aplasia
Homo sapiens (human)
DOID:0060284
  • paroxysmal nocturnal hemoglobinuria
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: August 19, 2024