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 7001 - 7025 of 7942 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism
DOID:1682
  • congenital heart disease
  • Aliases:
    • Congenital Heart Defects
    • Congenital anomaly of heart
    • Heart Malformation
    • congenital heart defect
    • heart defect
Rattus norvegicus (Norway rat)
DOID:0060050
  • autoimmune disease of blood
Xenopus tropicalis (tropical clawed frog)
DOID:0080941
  • acquired angioedema
Homo sapiens (human)
DOID:0060549
  • Barber-Say syndrome
Homo sapiens (human)
DOID:0060462
  • Desbuquois dysplasia
  • Aliases:
    • Desbuquois syndrome
    • micromelic dwarfism with vertebral and metaphyseal abnormalities and advanced carpotarsal ossification
Mus musculus (house mouse)
DOID:0060462
  • Desbuquois dysplasia
  • Aliases:
    • Desbuquois syndrome
    • micromelic dwarfism with vertebral and metaphyseal abnormalities and advanced carpotarsal ossification
Rattus norvegicus (Norway rat)
DOID:1168
  • familial hyperlipidemia
  • Aliases:
    • familial hyperlipoproteinemia
    • hyperlipemia
Saccharomyces cerevisiae S288C
DOID:10579
  • leukodystrophy
Saccharomyces cerevisiae S288C
DOID:0080547
  • metabolic dysfunction-associated steatohepatitis
  • Aliases:
    • MASH
    • NASH
    • non-alcoholic steatohepatitis
    • nonalcoholic steatohepatitis
Saccharomyces cerevisiae S288C
DOID:11612
  • polycystic ovary syndrome
  • Aliases:
    • Multicystic ovaries
    • PCOS
    • Polycystic Ovarian disease
    • Polycystic ovaries
    • Stein-Leventhal synd.
    • Stein-Leventhal syndrome
    • polycystic ovary
Saccharomyces cerevisiae S288C
DOID:0080201
  • Peters plus syndrome
  • Aliases:
    • Krause-Kivlin syndrome
    • Peters anomaly-short limb dwarfism syndrome
    • Peters-plus syndrome
Caenorhabditis elegans
DOID:9870
  • galactosemia
  • Aliases:
    • Galactosaemia
    • Galactose intolerance
Caenorhabditis elegans
DOID:0111459
  • classic galactosemia
  • Aliases:
    • GALT deficiency
    • galactose-1-phosphate uridyltransferase deficiency
    • galactosemia type 1
Caenorhabditis elegans
DOID:2978
  • carbohydrate metabolic disorder
  • Aliases:
    • disorder of carbohydrate transport and metabolism
    • inborn carbohydrate metabolism disorder
    • inborn errors of carbohydrate metabolism
Caenorhabditis elegans
DOID:0080554
  • congenital disorder of glycosylation Ib
  • Aliases:
    • congenital disorder of glycosylation 1b
Caenorhabditis elegans
DOID:1591
  • renovascular hypertension
Saccharomyces cerevisiae S288C
DOID:13413
  • hepatic encephalopathy
  • Aliases:
    • Portal-systemic encephalopathy
Saccharomyces cerevisiae S288C
DOID:9279
  • hyperhomocysteinemia
Saccharomyces cerevisiae S288C
DOID:13628
  • favism
Saccharomyces cerevisiae S288C
DOID:2383
  • neonatal jaundice
  • Aliases:
    • neonatal hyperbilirubinemia
    • neonatal icterus
Saccharomyces cerevisiae S288C
DOID:557
  • kidney disease
  • Aliases:
    • impaired renal function disease
    • nephropathy
Saccharomyces cerevisiae S288C
DOID:6713
  • cerebrovascular disease
  • Aliases:
    • CVA
    • cerebrovascular disorder
    • stroke
Saccharomyces cerevisiae S288C
DOID:14067
  • Plasmodium falciparum malaria
  • Aliases:
    • Malaria fever, subtertian
    • falciparum malaria
    • malignant tertian fever
Saccharomyces cerevisiae S288C
DOID:0050328
  • congenital hypothyroidism
Saccharomyces cerevisiae S288C
DOID:9281
  • phenylketonuria
  • Aliases:
    • Folling's disease
    • PKU
    • maternal phenylketonuria
    • phenylalaninemia
Saccharomyces cerevisiae S288C

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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