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 11051 - 11075 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲ Source
DOID:0080154
  • short chain acyl-CoA dehydrogenase deficiency
Mus musculus (house mouse)
DOID:11981
  • morbid obesity
  • Aliases:
    • Severe obesity
Mus musculus (house mouse)
DOID:0070054
  • Vulto-van Silfout-de Vries syndrome
  • Aliases:
    • IDDISBAS
    • MRD24
    • VSVS
    • autosomal dominant mental retardation 24
    • autosomal dominant non-syndromic intellectual disability 24
    • intellectual developmental disorder with impaired expressive speech and behavioral abnormalities, with or without seizures
Mus musculus (house mouse)
DOID:0050699
  • Dent disease
  • Aliases:
    • Dent disease 1
    • Dent disease 2
    • Dent's disease
Mus musculus (house mouse)
DOID:0110649
  • long QT syndrome 8
  • Aliases:
    • LQT8
Mus musculus (house mouse)
DOID:2121
  • ectodermal dysplasia
  • Aliases:
    • Congenital ectodermal defect
    • Congenital ectodermal dysplasia
Mus musculus (house mouse)
DOID:4990
  • essential tremor
  • Aliases:
    • benign essential tremor
    • essential hereditary tremor
    • shaky hand syndrome
Mus musculus (house mouse)
DOID:10605
  • short bowel syndrome
  • Aliases:
    • acquired short bowel syndrome
    • short gut syndrome
Mus musculus (house mouse)
DOID:0050461
  • aspartylglucosaminuria
  • Aliases:
    • aspartylglucosaminidase deficiency
    • aspartylglycosaminuria
    • glycosylasparaginase deficiency
Mus musculus (house mouse)
DOID:0060193
  • amyotrophic lateral sclerosis type 1
  • Aliases:
    • ALS1
    • amyotrophic lateral sclerosis 1
Mus musculus (house mouse)
DOID:10024
  • migraine with aura
  • Aliases:
    • classic migraine
Mus musculus (house mouse)
DOID:14320
  • generalized anxiety disorder
Mus musculus (house mouse)
DOID:768
  • retinoblastoma
  • Aliases:
    • RB
    • RB - Retinoblastoma
    • neuroblastoma of Retina
Mus musculus (house mouse)
DOID:0080411
  • familial adenomatous polyposis 3
Mus musculus (house mouse)
DOID:397
  • restrictive cardiomyopathy
  • Aliases:
    • Cardiomyopathy, constrictive
    • primary restrictive cardiomyopathy
Mus musculus (house mouse)
DOID:0110639
  • congenital muscular dystrophy due to integrin alpha-7 deficiency
  • Aliases:
    • congenital muscular dystrophy with ITGA7 deficiency
    • congenital muscular dystrophy with integrin alpha-7 deficiency
    • congenital myopathy due to integrin alpha-7 deficiency
Mus musculus (house mouse)
DOID:0080439
  • developmental and epileptic encephalopathy 14
  • Aliases:
    • DEE14
    • early infantile epileptic encephalopathy 14
Mus musculus (house mouse)
DOID:0080027
  • spondyloepimetaphyseal dysplasia
Mus musculus (house mouse)
DOID:13336
  • congenital toxoplasmosis
  • Aliases:
    • Toxoplasmosis - congen.
Mus musculus (house mouse)
DOID:8886
  • chorioretinitis
  • Aliases:
    • retinochoroiditis
Mus musculus (house mouse)
DOID:12185
  • otosclerosis
Mus musculus (house mouse)
DOID:0111138
  • congenital generalized lipodystrophy type 4
  • Aliases:
    • Berardinelli-Seip congenital lipodystrophy type 4 with muscular dystrophy
    • congenital generalised lipodystrophy type 4
    • generalised congenital lipodystrophy type 4
    • generalised congenital lipodystrophy with myopathy
    • generalized congenital lipodystrophy type 4
    • generalized congenital lipodystrophy with myopathy
Mus musculus (house mouse)
DOID:0080925
  • cytochrome P450 oxidoreductase deficiency
Mus musculus (house mouse)
DOID:0111438
  • optic atrophy 5
  • Aliases:
    • OPA5
Mus musculus (house mouse)
DOID:3213
  • demyelinating disease
  • Aliases:
    • demyelinating disorder
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