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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 6226 - 6250 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲ Source
DOID:0080470
  • developmental and epileptic encephalopathy 36
  • Aliases:
    • congenital disorder of glycosylation, type Is
    • early infantile epileptic encephalopathy 36
Mus musculus (house mouse)
DOID:14227
  • azoospermia
Mus musculus (house mouse)
DOID:0060001
  • withdrawal disorder
Mus musculus (house mouse)
DOID:3021
  • acute kidney failure
Mus musculus (house mouse)
DOID:11727
  • facioscapulohumeral muscular dystrophy
  • Aliases:
    • Landouzy Dejerine muscular dystrophy
    • Landouzy-Dejerine muscular dystrophy
    • Muscular dystrophy, Landouzy-Dejerine
Mus musculus (house mouse)
DOID:1993
  • rectum cancer
  • Aliases:
    • carcinoma of rectum
    • carcinoma of the rectum
    • malignant Rectal tumor
    • malignant neoplasm of rectum
    • malignant rectum tumor
    • malignant tumor of rectum
    • rectal cancer
Mus musculus (house mouse)
DOID:11506
  • suppurative otitis media
  • Aliases:
    • Otitis media with effusion - purulent
    • Purulent otitis media
Mus musculus (house mouse)
DOID:0002116
  • pterygium
  • Aliases:
    • surfer's eye
Mus musculus (house mouse)
DOID:0050524
  • maturity-onset diabetes of the young
  • Aliases:
    • MODY
    • Mason-type diabetes
Mus musculus (house mouse)
DOID:0050589
  • inflammatory bowel disease
Mus musculus (house mouse)
DOID:0111240
  • congenital muscular dystrophy-dystroglycanopathy type A2
  • Aliases:
    • MDDGA2
    • Walker-Warburg syndrome or muscle-eye-brain disease, POMT2-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A2
Mus musculus (house mouse)
DOID:0110242
  • cataract 13 with adult i phenotype
  • Aliases:
    • CTRCT13
Mus musculus (house mouse)
DOID:0070295
  • primary autosomal dominant microcephaly 18
  • Aliases:
    • MCPH18
Mus musculus (house mouse)
DOID:1227
  • neutropenia
Mus musculus (house mouse)
DOID:0080855
  • Parkinsonism
Mus musculus (house mouse)
DOID:2671
  • transitional cell carcinoma
  • Aliases:
    • transitional carcinoma
    • transitional cell tumor
    • urothelial cell carcinoma
Mus musculus (house mouse)
DOID:12399
  • pathological gambling
  • Aliases:
    • Compulsive gambling
Mus musculus (house mouse)
DOID:0110299
  • autosomal recessive limb-girdle muscular dystrophy type 2I
  • Aliases:
    • LGMD2I
    • Limb-girdle muscular dystrophy due to FKRP deficiency
    • MDDGC5
    • muscular dystrophy limb-girdle type 2I
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C 5
    • muscular dystrophy-dystroglycanopathy limb-girdle FRKP-related
Mus musculus (house mouse)
DOID:0050650
  • familial atrial fibrillation
  • Aliases:
    • ATFB
Mus musculus (house mouse)
DOID:3748
  • esophagus squamous cell carcinoma
  • Aliases:
    • SCC of esophagus
    • SCC of oesophagus
    • oesophagus squamous cell carcinoma
Mus musculus (house mouse)
DOID:5742
  • pancreatic acinar cell adenocarcinoma
  • Aliases:
    • pancreatic acinar cell carcinoma
Mus musculus (house mouse)
DOID:0070342
  • adult-onset type II citrullinemia
  • Aliases:
    • citrin deficiency
Mus musculus (house mouse)
DOID:0060256
  • Dowling-Degos disease
  • Aliases:
    • dark dot disease
    • reticular pigment anomaly of flexures
Mus musculus (house mouse)
DOID:0080411
  • familial adenomatous polyposis 3
Mus musculus (house mouse)
DOID:3534
  • Lafora disease
  • Aliases:
    • Lafora Progressive Myoclonic Epilepsy
    • Lafora's disease
    • MYOCLONIC EPILEPSY OF LAFORA
Mus musculus (house mouse)
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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