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 all 23 entries
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism
DOID:1443
  • cerebral degeneration
  • Aliases:
    • Brain degeneration
Homo sapiens (human)
DOID:0080567
  • congenital disorder of glycosylation Ip
  • Aliases:
    • congenital disorder of glycosylation 1p
Danio rerio (zebrafish)
DOID:0080567
  • congenital disorder of glycosylation Ip
  • Aliases:
    • congenital disorder of glycosylation 1p
Xenopus laevis (African clawed frog)
DOID:0080567
  • congenital disorder of glycosylation Ip
  • Aliases:
    • congenital disorder of glycosylation 1p
Drosophila melanogaster (fruit fly)
DOID:0080567
  • congenital disorder of glycosylation Ip
  • Aliases:
    • congenital disorder of glycosylation 1p
Mus musculus (house mouse)
DOID:0080567
  • congenital disorder of glycosylation Ip
  • Aliases:
    • congenital disorder of glycosylation 1p
Saccharomyces cerevisiae S288C
DOID:0080567
  • congenital disorder of glycosylation Ip
  • Aliases:
    • congenital disorder of glycosylation 1p
Rattus norvegicus (Norway rat)
DOID:0080567
  • congenital disorder of glycosylation Ip
  • Aliases:
    • congenital disorder of glycosylation 1p
Homo sapiens (human)
DOID:0080567
  • congenital disorder of glycosylation Ip
  • Aliases:
    • congenital disorder of glycosylation 1p
Xenopus tropicalis (tropical clawed frog)
DOID:0050570
  • congenital disorder of glycosylation type I
Homo sapiens (human)
DOID:5212
  • congenital disorder of glycosylation
  • Aliases:
    • carbohydrate-deficient glycoprotein syndrome
Homo sapiens (human)
DOID:1826
  • epilepsy
  • Aliases:
    • epilepsy syndrome
    • epileptic syndrome
Homo sapiens (human)
DOID:9837
  • hypertropia
Homo sapiens (human)
DOID:655
  • inherited metabolic disorder
  • Aliases:
    • Inborn Errors of Metabolism
    • Metabolic hereditary disorder
    • inborn metabolism disorder
Homo sapiens (human)
DOID:1059
  • intellectual disability
Homo sapiens (human)
DOID:8927
  • learning disability
  • Aliases:
    • Academic skill disorder
    • learning disorder
Homo sapiens (human)
DOID:9306
  • mechanical strabismus
Homo sapiens (human)
DOID:10907
  • microcephaly
  • Aliases:
    • Microcephalus
    • microencephaly
Homo sapiens (human)
DOID:539
  • ophthalmoplegia
  • Aliases:
    • Total ophthalmoplegia
    • extraocular muscle paralysis
    • eye movement paralysis
    • oculomotor paralysis
Homo sapiens (human)
DOID:0060249
  • scoliosis
Homo sapiens (human)
DOID:10003
  • sensorineural hearing loss
  • Aliases:
    • High Frequency Hearing Loss
    • High frequency deafness
    • Perceptive deafness
    • Perceptive hearing loss
    • Perceptive hearing loss or deafness
    • Sensorineural Deafness
    • Sensory hearing loss
    • central hearing loss
    • high-frequency hearing loss
Homo sapiens (human)
DOID:540
  • strabismus
Homo sapiens (human)
DOID:11832
  • visual epilepsy
  • Aliases:
    • epilepsy, visual
Homo sapiens (human)

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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: August 19, 2024