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 4376 - 4400 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism
DOID:1563
  • dermatomycosis
Homo sapiens (human)
DOID:2058
  • chronic mucocutaneous candidiasis
Homo sapiens (human)
DOID:1562
  • chromoblastomycosis
  • Aliases:
    • Chromomycosis
    • Mossy foot disease
Homo sapiens (human)
DOID:0060362
  • punctate palmoplantar keratoderma type III
  • Aliases:
    • acrokeratoelastoidosis of Costa
    • punctate palmoplantar hyperkeratosis type 3
    • punctate palmoplantar keratoderma type 3
Homo sapiens (human)
DOID:0111633
  • congenital sucrase-isomaltase deficiency
  • Aliases:
    • CSID
    • SI deficiency
    • congenital sucrase-isomaltose malabsorption
    • congenital sucrose intolerance
    • disaccharide intolerance
Homo sapiens (human)
DOID:0060307
  • autosomal dominant intellectual developmental disorder
  • Aliases:
    • autosomal dominant mental retardation
    • autosomal dominant non-syndromic mental retardation
Homo sapiens (human)
DOID:0070034
  • autosomal dominant intellectual developmental disorder 4
  • Aliases:
    • MRD4
    • autosomal dominant mental retardation 4
    • autosomal dominant non-syndromic intellectual disability 4
Homo sapiens (human)
DOID:0080753
  • keratosis follicularis spinulosa decalvans
Homo sapiens (human)
DOID:0070311
  • oligoasthenoteratozoospermia
  • Aliases:
    • OAT
    • oligoasthenoteratospermia
Homo sapiens (human)
DOID:0080414
  • developmental and epileptic encephalopathy 15
  • Aliases:
    • DEE15
    • early infantile epileptic encephalopathy 15
Homo sapiens (human)
DOID:0081180
  • autosomal recessive intellectual developmental disorder 12
Homo sapiens (human)
DOID:0090044
  • dystonia 9
Homo sapiens (human)
DOID:0111313
  • idiopathic generalized epilepsy 12
  • Aliases:
    • EIG12
Homo sapiens (human)
DOID:10486
  • intestinal atresia
Homo sapiens (human)
DOID:0060858
  • hypotonia-cystinuria syndrome
  • Aliases:
    • cystinuria with mitochondrial disease
Homo sapiens (human)
DOID:0080587
  • congenital myasthenic syndrome 22
Homo sapiens (human)
DOID:0080899
  • lung pleomorphic carcinoma
Homo sapiens (human)
DOID:0050157
  • cryptogenic organizing pneumonia
  • Aliases:
    • BOOP
    • Cryptogenic organising pneumonitis
    • Cryptogenic organizing pneumonitis
    • bronchiolitis obliterans organising pneumonia
    • bronchiolitis obliterans organizing pneumonia
    • cryptogenic organising pneumonia
    • idiopathic bronchiolitis obliterans with organising pneumonia
    • idiopathic bronchiolitis obliterans with organizing pneumonia
Homo sapiens (human)
DOID:96
  • staphyloenterotoxemia
  • Aliases:
    • Staphylococcal food poisoning
    • Staphylococcal toxaemia due to food
    • staphyloenterotoxicosis
Homo sapiens (human)
DOID:0111619
  • combined D-2- and L-2-hydroxyglutaric aciduria
  • Aliases:
    • D,L-2-HGA
    • D,L-2-hydroxyglutaric acidemia
    • D,L-2-hydroxyglutaric aciduria
    • combined D,L-2-hydroxyglutaric aciduria
    • combined D-2-hydroxyglutaric acidemia and L-2-hydroxyglutaric acidemia
    • combined D-2-hydroxyglutaric aciduria and L-2-hydroxyglutaric aciduria
Homo sapiens (human)
DOID:990
  • congenital heart block
Homo sapiens (human)
DOID:8553
  • pyoderma gangrenosum
Homo sapiens (human)
DOID:0050169
  • cutaneous lupus erythematosus
Homo sapiens (human)
DOID:0081427
  • autosomal recessive distal hereditary motor neuronopathy 8
  • Aliases:
    • SORDD
    • sorbitol dehydrogenase deficiency with peripheral neuropathy
Homo sapiens (human)
DOID:0081376
  • obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy
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