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 October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 10301 - 10325 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲ Source
DOID:3635
  • congenital myasthenic syndrome
Mus musculus (house mouse)
DOID:0111153
  • congenital mirror movement disorder
  • Aliases:
    • familial congenital controlateral synkinesia
    • familial congenital mirror movements
    • hereditary congenital controlateral synkinesia
    • hereditary congenital mirror movements
    • isolated congenital controlateral synkinesia
    • isolated congenital mirror movements
Mus musculus (house mouse)
DOID:2383
  • neonatal jaundice
  • Aliases:
    • neonatal hyperbilirubinemia
    • neonatal icterus
Mus musculus (house mouse)
DOID:0060186
  • chemical colitis
Mus musculus (house mouse)
DOID:5425
  • ovarian hyperstimulation syndrome
  • Aliases:
    • secondary Meig's syndrome
Mus musculus (house mouse)
DOID:4449
  • macular retinal edema
  • Aliases:
    • macular edema
    • macular oedema
    • macular retinal oedema
Mus musculus (house mouse)
DOID:0081344
  • congenital myopathy 9B
Mus musculus (house mouse)
DOID:0110459
  • dilated cardiomyopathy 1FF
  • Aliases:
    • CMD1FF
Mus musculus (house mouse)
DOID:0110156
  • Charcot-Marie-Tooth disease type 2B1
  • Aliases:
    • CMT2B1
    • Charcot-Marie-Tooth disease neuronal type 2B1
    • Charcot-Marie-Tooth neuropathy type 2B1
    • autosomal recessive Charcot-Marie-Tooth disease type 2B1
    • autosomal recessive axonal CMT4C1
    • autosomal recessive axonal Charcot-Marie-Tooth disease type 2B1
Mus musculus (house mouse)
DOID:0080832
  • mild cognitive impairment
Mus musculus (house mouse)
DOID:0111258
  • pentosuria
  • Aliases:
    • L-xylulose reductase deficiency
    • L-xylulosuria
    • PNTSU
    • essential pentosuria
    • xylitol dehydrogenase deficiency
Mus musculus (house mouse)
DOID:0110383
  • retinitis pigmentosa 7
  • Aliases:
    • RP7
Mus musculus (house mouse)
DOID:3650
  • lactic acidosis
Mus musculus (house mouse)
DOID:4252
  • Alexander disease
  • Aliases:
    • Alexander's disease
Mus musculus (house mouse)
DOID:1070
  • primary open angle glaucoma
  • Aliases:
    • chronic simple glaucoma
Mus musculus (house mouse)
DOID:0080918
  • polymicrogyria
Mus musculus (house mouse)
DOID:0070346
  • neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies
Mus musculus (house mouse)
DOID:0110895
  • inflammatory bowel disease 14
  • Aliases:
    • IBD14
Mus musculus (house mouse)
DOID:4905
  • pancreatic carcinoma
  • Aliases:
    • Exocrine pancreas carcinoma
    • carcinoma of pancreas
Mus musculus (house mouse)
DOID:0110054
  • amelogenesis imperfecta type 1A
  • Aliases:
    • AI1A
    • amelogenesis imperfecta hypoplastic type IA
    • amelogenesis imperfecta type IA
Mus musculus (house mouse)
DOID:0111696
  • familial adult myoclonic epilepsy 6
  • Aliases:
    • BAFME6
    • FAME6
    • FCMTE6
    • benign adult familial myoclonic epilepsy 6
    • familial cortical myoclonic tremor and epilepsy 6
Mus musculus (house mouse)
DOID:11949
  • Creutzfeldt-Jakob disease
  • Aliases:
    • CJD
    • Creutzfeldt Jacob syndrome
    • Creutzfeldt Jakob disease
    • Creutzfeldt-Jacob disease
    • Jakob-Creutzfeldt disease
    • Subacute spongiform encephalopathy
    • Transmissible virus dementia
Mus musculus (house mouse)
DOID:0111181
  • familial hemiplegic migraine 1
  • Aliases:
    • FHM1
    • MHP1
    • familial hemiplegic migraine1 with progressive cerebellar ataxia
Mus musculus (house mouse)
DOID:12399
  • pathological gambling
  • Aliases:
    • Compulsive gambling
Mus musculus (house mouse)
DOID:0080726
  • Ehlers-Danlos syndrome classic type 2
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: December 9, 2024