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 126 - 150 of 7942 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism
DOID:0050476
  • Barth syndrome
  • Aliases:
    • 3-methylglutaconicaciduria type 2
    • 3-methylglutaconicaciduria type II
    • MGA Type 2
    • MGA type II
Homo sapiens (human)
DOID:0050477
  • Liddle syndrome
  • Aliases:
    • Liddle's syndrome
    • Pseudoaldosteronism
Homo sapiens (human)
DOID:0050486
  • exanthem
Homo sapiens (human)
DOID:0050495
  • exanthema subitum
  • Aliases:
    • Roseola Infantum
    • Sixth Disease
Homo sapiens (human)
DOID:0050508
  • variola major
Homo sapiens (human)
DOID:0050523
  • adult T-cell leukemia/lymphoma
  • Aliases:
    • Adult T-cell leukemia/lymphoma (HTLV-1 positive)
    • adult T-cell leukemia
Drosophila melanogaster (fruit fly)
DOID:0050523
  • adult T-cell leukemia/lymphoma
  • Aliases:
    • Adult T-cell leukemia/lymphoma (HTLV-1 positive)
    • adult T-cell leukemia
Homo sapiens (human)
DOID:0050524
  • maturity-onset diabetes of the young
  • Aliases:
    • MODY
    • Mason-type diabetes
Drosophila melanogaster (fruit fly)
DOID:0050524
  • maturity-onset diabetes of the young
  • Aliases:
    • MODY
    • Mason-type diabetes
Mus musculus (house mouse)
DOID:0050524
  • maturity-onset diabetes of the young
  • Aliases:
    • MODY
    • Mason-type diabetes
Rattus norvegicus (Norway rat)
DOID:0050524
  • maturity-onset diabetes of the young
  • Aliases:
    • MODY
    • Mason-type diabetes
Danio rerio (zebrafish)
DOID:0050524
  • maturity-onset diabetes of the young
  • Aliases:
    • MODY
    • Mason-type diabetes
Saccharomyces cerevisiae S288C
DOID:0050524
  • maturity-onset diabetes of the young
  • Aliases:
    • MODY
    • Mason-type diabetes
Homo sapiens (human)
DOID:0050526
  • Gamstorp-Wohlfart syndrome
  • Aliases:
    • autosomal recessive neuromyotonia and axonal neuropathy
    • myokymia, myotonia and muscle wasting
Homo sapiens (human)
DOID:0050527
  • obsolete familial hypertriglyceridemia
Homo sapiens (human)
DOID:0050534
  • congenital stationary night blindness
  • Aliases:
    • congenital essential nyctalopia
Homo sapiens (human)
DOID:0050535
  • exudative vitreoretinopathy
  • Aliases:
    • FEVR
    • familial exudative vitreoretinopathy
Mus musculus (house mouse)
DOID:0050535
  • exudative vitreoretinopathy
  • Aliases:
    • FEVR
    • familial exudative vitreoretinopathy
Homo sapiens (human)
DOID:0050536
  • obsolete SC phocomelia syndrome
  • Aliases:
    • Hypomelia Hypotrichosis Facial hemangioma syndrome
    • SC PSEUDOTHALIDOMIDE SYNDROME
Homo sapiens (human)
DOID:0050539
  • Charcot-Marie-Tooth disease type 2
  • Aliases:
    • hereditary motor and sensory neuropathy Guadalajara neuronal type
    • hereditary motor and sensory neuropathy Okinawa type
    • hereditary motor and sensory neuropathy type 2
Homo sapiens (human)
DOID:0050540
  • Charcot-Marie-Tooth disease type 3
  • Aliases:
    • DEJERINE-SOTTAS NEUROPATHY
    • DEJERINE-SOTTAS SYNDROME
Homo sapiens (human)
DOID:0050541
  • Charcot-Marie-Tooth disease type 4
  • Aliases:
    • hereditary motor and sensory neuropathy
Homo sapiens (human)
DOID:0050542
  • Charcot-Marie-Tooth disease type X
Homo sapiens (human)
DOID:0050545
  • visceral heterotaxy
  • Aliases:
    • heterotaxia
    • situs ambiguus
Caenorhabditis elegans
DOID:0050545
  • visceral heterotaxy
  • Aliases:
    • heterotaxia
    • situs ambiguus
Drosophila melanogaster (fruit fly)

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Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024