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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 January 28, 2025
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 1426 - 1450 of 5716 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism Source
DOID:0080154
  • short chain acyl-CoA dehydrogenase deficiency
Homo sapiens (human)
DOID:0080154
  • short chain acyl-CoA dehydrogenase deficiency
Mus musculus (house mouse)
DOID:0080155
  • very long chain acyl-CoA dehydrogenase deficiency
  • Aliases:
    • VLCAD deficiency
Mus musculus (house mouse)
DOID:0080155
  • very long chain acyl-CoA dehydrogenase deficiency
  • Aliases:
    • VLCAD deficiency
Homo sapiens (human)
DOID:0080156
  • X-linked adrenal hypoplasia congenita
  • Aliases:
    • congenital adrenal hypoplasia
Homo sapiens (human)
DOID:0080158
  • herpes simplex virus keratitis
  • Aliases:
    • dendritic keratitis
Homo sapiens (human)
DOID:0080159
  • Cryptococcal meningitis
Homo sapiens (human)
DOID:0080160
  • Cytomegalovirus retinitis
  • Aliases:
    • CMV retinitis
Homo sapiens (human)
DOID:0080162
  • lupus nephritis
Homo sapiens (human)
DOID:0080163
  • otulipenia
  • Aliases:
    • autoinflammation, panniculitis and dermatosis syndrome
    • otulin-related autoinflammatory syndrome
Homo sapiens (human)
DOID:0080170
  • normophosphatemic familial tumoral calcinosis
Homo sapiens (human)
DOID:0080171
  • esophageal atresia/tracheoesophageal fistula
  • Aliases:
    • esophageal atresia and/or tracheoesophageal fistula
    • tracheoesophageal fistula with or without esohageal atresia
Mus musculus (house mouse)
DOID:0080176
  • meningococcal meningitis
Homo sapiens (human)
DOID:0080177
  • hepatic veno-occlusive disease
  • Aliases:
    • veno-occlusive disease
Homo sapiens (human)
DOID:0080179
  • haemophilus meningitis
Homo sapiens (human)
DOID:0080181
  • PHARC syndrome
  • Aliases:
    • polyneyropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract
Danio rerio (zebrafish)
DOID:0080181
  • PHARC syndrome
  • Aliases:
    • polyneyropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract
Mus musculus (house mouse)
DOID:0080181
  • PHARC syndrome
  • Aliases:
    • polyneyropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract
Homo sapiens (human)
DOID:0080187
  • chronic neutrophilic leukemia
Homo sapiens (human)
DOID:0080188
  • chronic myelomonocytic leukemia
Homo sapiens (human)
DOID:0080188
  • chronic myelomonocytic leukemia
Mus musculus (house mouse)
DOID:0080191
  • PTEN hamartoma tumor syndrome
Homo sapiens (human)
DOID:0080195
  • Marinesco-Sjogren syndrome
  • Aliases:
    • Garland-Moorhouse syndrome
    • Marinesco-Garland syndrome
    • Oligophrenic cerebellolenticular degeneration
    • hereditary oligophrenic cerebello-lental degeneration
Saccharomyces cerevisiae S288C
DOID:0080196
  • mandibulofacial dysostosis, Guion-Almeida type
  • Aliases:
    • MFDM syndrome
    • mandibulofacial dysostosis with microcephaly
    • mandibulofacial dysostosis-microcephaly syndrome
Homo sapiens (human)
DOID:0080197
  • congenital muscular dystrophy with cataracts and intellectual disability
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: December 8, 2025