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 July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 2226 - 2250 of 7942 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:2671
  • transitional cell carcinoma
  • Aliases:
    • transitional carcinoma
    • transitional cell tumor
    • urothelial cell carcinoma
Saccharomyces cerevisiae S288C
DOID:3314
  • angiomyolipoma
Saccharomyces cerevisiae S288C
DOID:3525
  • middle cerebral artery infarction
Saccharomyces cerevisiae S288C
DOID:6933
  • bladder transitional cell papilloma
  • Aliases:
    • Urothelial papilloma
    • bladder papilloma
    • transitional cell papilloma of bladder
    • urinary bladder Urothelial papilloma
Homo sapiens (human)
DOID:6217
  • gastric diffuse adenocarcinoma
Homo sapiens (human)
DOID:0070468
  • Yoon-Bellen neurodevelopmental syndrome
  • Aliases:
    • YOBELN
Homo sapiens (human)
DOID:0081326
  • oxoglutarate dehydrogenase deficiency
  • Aliases:
    • Oxoglutaric aciduria
    • alpha-ketoglutarate dehydrogenase deficiency
Homo sapiens (human)
DOID:14250
  • Down syndrome
  • Aliases:
    • Complete trisomy 21 syndrome
    • Down's syndrome
    • Down's syndrome - trisomy 21
    • Downs syndrome
    • G Trisomy
    • trisomy 21 syndrome
Drosophila melanogaster (fruit fly)
DOID:0080411
  • familial adenomatous polyposis 3
Mus musculus (house mouse)
DOID:0112313
  • brain small vessel disease
Rattus norvegicus (Norway rat)
DOID:10762
  • portal hypertension
Rattus norvegicus (Norway rat)
DOID:0112313
  • brain small vessel disease
Mus musculus (house mouse)
DOID:10762
  • portal hypertension
Mus musculus (house mouse)
DOID:1825
  • childhood absence epilepsy
  • Aliases:
    • petit mal seizure
    • pyknolepsy
Mus musculus (house mouse)
DOID:3328
  • temporal lobe epilepsy
  • Aliases:
    • epilepsy, temporal lobe
Mus musculus (house mouse)
DOID:0070113
  • Niemann-Pick disease type C1
  • Aliases:
    • NPC1
Mus musculus (house mouse)
DOID:14504
  • Niemann-Pick disease
  • Aliases:
    • Sphingomyelinase Deficiency Disease
    • lipoid histiocytosis
    • sphingomyelin lipidosis
Mus musculus (house mouse)
DOID:11198
  • DiGeorge syndrome
  • Aliases:
    • 22q11.2 deletion syndrome
    • DiGeorge sequence
    • DiGeorge's syndrome
    • Pharyngeal pouch syndrome
Rattus norvegicus (Norway rat)
DOID:12716
  • newborn respiratory distress syndrome
  • Aliases:
    • HMD - Hyaline membrane disease
    • Neonatal respiratory Distress syndrome
    • hyaline membrane disease
    • pulmonary hyaline membrane disease
    • pulmonary hypoperfusion syndrome of newborn
    • respiratory distress syndrome of newborn
Rattus norvegicus (Norway rat)
DOID:0081210
  • autosomal recessive intellectual developmental disorder 46
Rattus norvegicus (Norway rat)
DOID:14227
  • azoospermia
Rattus norvegicus (Norway rat)
DOID:0081210
  • autosomal recessive intellectual developmental disorder 46
Mus musculus (house mouse)
DOID:12716
  • newborn respiratory distress syndrome
  • Aliases:
    • HMD - Hyaline membrane disease
    • Neonatal respiratory Distress syndrome
    • hyaline membrane disease
    • pulmonary hyaline membrane disease
    • pulmonary hypoperfusion syndrome of newborn
    • respiratory distress syndrome of newborn
Mus musculus (house mouse)
DOID:11198
  • DiGeorge syndrome
  • Aliases:
    • 22q11.2 deletion syndrome
    • DiGeorge sequence
    • DiGeorge's syndrome
    • Pharyngeal pouch syndrome
Mus musculus (house mouse)
DOID:14227
  • azoospermia
Mus musculus (house mouse)

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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