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 4526 - 4550 of 7942 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism
DOID:557
  • kidney disease
  • Aliases:
    • impaired renal function disease
    • nephropathy
Rattus norvegicus (Norway rat)
DOID:12365
  • malaria
  • Aliases:
    • induced malaria
Rattus norvegicus (Norway rat)
DOID:0050328
  • congenital hypothyroidism
Rattus norvegicus (Norway rat)
DOID:13580
  • cholestasis
  • Aliases:
    • Obstruction of bile duct
    • bile occlusion
Rattus norvegicus (Norway rat)
DOID:9281
  • phenylketonuria
  • Aliases:
    • Folling's disease
    • PKU
    • maternal phenylketonuria
    • phenylalaninemia
Rattus norvegicus (Norway rat)
DOID:13413
  • hepatic encephalopathy
  • Aliases:
    • Portal-systemic encephalopathy
Rattus norvegicus (Norway rat)
DOID:6713
  • cerebrovascular disease
  • Aliases:
    • CVA
    • cerebrovascular disorder
    • stroke
Rattus norvegicus (Norway rat)
DOID:2383
  • neonatal jaundice
  • Aliases:
    • neonatal hyperbilirubinemia
    • neonatal icterus
Rattus norvegicus (Norway rat)
DOID:13628
  • favism
Rattus norvegicus (Norway rat)
DOID:224
  • transient cerebral ischemia
  • Aliases:
    • TIA
    • TIA - Transient ischaemic attack
    • Transient cerebral ischaemia
    • Transient ischemic attacks
    • transient ischemic attack
Mus musculus (house mouse)
DOID:2861
  • congenital nonspherocytic hemolytic anemia
  • Aliases:
    • HNSHA
    • congenital nonspherocytic hemolytic anaemia
    • hereditary nonspherocytic hemolytic anaemia
    • hereditary nonspherocytic hemolytic anemia
Mus musculus (house mouse)
DOID:2355
  • anemia
  • Aliases:
    • anaemia
Mus musculus (house mouse)
DOID:557
  • kidney disease
  • Aliases:
    • impaired renal function disease
    • nephropathy
Mus musculus (house mouse)
DOID:0050328
  • congenital hypothyroidism
Mus musculus (house mouse)
DOID:13580
  • cholestasis
  • Aliases:
    • Obstruction of bile duct
    • bile occlusion
Mus musculus (house mouse)
DOID:12365
  • malaria
  • Aliases:
    • induced malaria
Mus musculus (house mouse)
DOID:2383
  • neonatal jaundice
  • Aliases:
    • neonatal hyperbilirubinemia
    • neonatal icterus
Mus musculus (house mouse)
DOID:13413
  • hepatic encephalopathy
  • Aliases:
    • Portal-systemic encephalopathy
Mus musculus (house mouse)
DOID:13628
  • favism
Mus musculus (house mouse)
DOID:9281
  • phenylketonuria
  • Aliases:
    • Folling's disease
    • PKU
    • maternal phenylketonuria
    • phenylalaninemia
Mus musculus (house mouse)
DOID:6713
  • cerebrovascular disease
  • Aliases:
    • CVA
    • cerebrovascular disorder
    • stroke
Mus musculus (house mouse)
DOID:1574
  • alcohol use disorder
  • Aliases:
    • Ethanol abuse
    • alcohol abuse
Saccharomyces cerevisiae S288C
DOID:13366
  • Stiff-Person syndrome
  • Aliases:
    • Stiff-man syndrome
    • stiff man syndrome
Homo sapiens (human)
DOID:0050669
  • spastic cerebral palsy
Homo sapiens (human)
DOID:9274
  • hyperlysinemia
Homo sapiens (human)

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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