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 6876 - 6900 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:0050424
  • familial adenomatous polyposis
  • Aliases:
    • adenomatous polyposis of the colon
Mus musculus (house mouse)
DOID:10763
  • hypertension
  • Aliases:
    • HTN
    • hyperpiesia
    • vascular hypertensive disorder
Mus musculus (house mouse)
DOID:0050802
  • Ehlers-Danlos syndrome spondylodysplastic type 2
  • Aliases:
    • EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 2
    • Ehlers-Danlos syndrome progeroid type
Mus musculus (house mouse)
DOID:0080345
  • blepharocheilodontic syndrome 1
Mus musculus (house mouse)
DOID:655
  • inherited metabolic disorder
  • Aliases:
    • Inborn Errors of Metabolism
    • Metabolic hereditary disorder
    • inborn metabolism disorder
Mus musculus (house mouse)
DOID:0080581
  • hyperekplexia 4
Mus musculus (house mouse)
DOID:0110893
  • inflammatory bowel disease 13
  • Aliases:
    • IBD13
Mus musculus (house mouse)
DOID:0050884
  • triosephosphate isomerase deficiency
  • Aliases:
    • Triose phosphate-isomerase deficiency
Mus musculus (house mouse)
DOID:0060237
  • Warburg micro syndrome
  • Aliases:
    • WARBM
    • Warburg-Sjo-Fledelius syndrome
    • micro syndrome
Mus musculus (house mouse)
DOID:0080026
  • otospondylomegaepiphyseal dysplasia, autosomal recessive
  • Aliases:
    • CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS
    • NANCE-INSLEY SYNDROME
    • NANCE-SWEENEY CHONDRODYSPLASIA
    • OSMEDB
Mus musculus (house mouse)
DOID:1933
  • Rubinstein-Taybi syndrome
  • Aliases:
    • Broad Thumb-Hallux syndrome
    • Rubinstein syndrome
    • proximal chromosome 16p13.3 deletion syndrome
Mus musculus (house mouse)
DOID:3669
  • intermittent claudication
  • Aliases:
    • Charcot's syndrome
Mus musculus (house mouse)
DOID:0080621
  • glucocorticoid deficiency 1
Mus musculus (house mouse)
DOID:0112083
  • nuclear type mitochondrial complex I deficiency 2
  • Aliases:
    • MC1DN2
Mus musculus (house mouse)
DOID:5733
  • salpingitis
Mus musculus (house mouse)
DOID:3113
  • papillary carcinoma
Mus musculus (house mouse)
DOID:0090132
  • complex cortical dysplasia with other brain malformations 7
  • Aliases:
    • CDCBM7
    • polymicrogyria due to TUBB2B mutation
Mus musculus (house mouse)
DOID:0060194
  • amyotrophic lateral sclerosis type 2
  • Aliases:
    • ALS2
    • amyotrophic lateral sclerosis 2
    • amyotrophic lateral sclerosis 2, juvenile
Mus musculus (house mouse)
DOID:0060370
  • Parkinson's disease 7
  • Aliases:
    • autosomal recessive early-onset Parkinson disease 7
    • autosomal recessive early-onset Parkinson's disease 7
Mus musculus (house mouse)
DOID:0050589
  • inflammatory bowel disease
Mus musculus (house mouse)
DOID:0050711
  • aceruloplasminemia
Mus musculus (house mouse)
DOID:0070519
  • early-onset vitamin B6-dependent epilepsy 4
  • Aliases:
    • AASA dehydrogenase deficiency
    • EPEO4
    • PDE-ALDH7A1
    • antiquitin deficiency
Mus musculus (house mouse)
DOID:3687
  • MELAS syndrome
  • Aliases:
    • MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES
Mus musculus (house mouse)
DOID:4257
  • Caffey disease
  • Aliases:
    • cortical congenital hyperostosis
    • infantile cortical hyperostosis
Mus musculus (house mouse)
DOID:5327
  • retinal detachment
Mus musculus (house mouse)

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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: December 9, 2024