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 4226 - 4250 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:0111909
  • autosomal dominant thrombophilia due to protein C deficiency
  • Aliases:
    • THPH3
    • autosomal dominant PROC deficiency
    • autosomal dominant protein C deficiency
Mus musculus (house mouse)
DOID:1928
  • Williams-Beuren syndrome
  • Aliases:
    • Fanconi Schlesinger syndrome
    • WBS
Mus musculus (house mouse)
DOID:0111960
  • immunodeficiency 15A
  • Aliases:
    • IMD15A
Mus musculus (house mouse)
DOID:1883
  • hepatitis C
  • Aliases:
    • NANBH
    • Viral hepatitis C
    • chronic hepatitis C
    • hepatitis C infection
    • hepatitis nonA nonB
Mus musculus (house mouse)
DOID:0080263
  • autosomal recessive nonsyndromic deafness 108
Mus musculus (house mouse)
DOID:0060887
  • ossification of the posterior longitudinal ligament of spine
  • Aliases:
    • OPLL
Mus musculus (house mouse)
DOID:0060780
  • congenital diarrhea 6
  • Aliases:
    • chronic diarrhea due to guanylate cyclase 2C overactivity
    • chronic diarrhoea due to guanylate cyclase 2C overactivity
    • congenital diarrhoea 6
Mus musculus (house mouse)
DOID:10283
  • prostate cancer
  • Aliases:
    • NGP - new growth of prostate
    • hereditary prostate cancer
    • malignant tumor of the prostate
    • prostate cancer, familial
    • prostate neoplasm
    • prostatic cancer
    • prostatic neoplasm
    • tumor of the prostate
Mus musculus (house mouse)
DOID:4988
  • alcoholic pancreatitis
Mus musculus (house mouse)
DOID:0080679
  • neuronal intestinal dysplasia type A
Mus musculus (house mouse)
DOID:0080227
  • autosomal dominant intellectual developmental disorder 55
  • Aliases:
    • autosomal dominant intellectual developmental disorder-55 with seizures
    • autosomal dominant mental retardation 55
Mus musculus (house mouse)
DOID:0110870
  • congenital stationary night blindness 1A
  • Aliases:
    • CSNB1A
    • NBMI
    • complete CSNB X-linked
    • congenital stationary night blindness 1A X-linked
    • congenital stationary night blindness with myopia
    • hemeralopia-myopia
    • myopia-night blindness
Mus musculus (house mouse)
DOID:0080570
  • congenital disorder of glycosylation It
  • Aliases:
    • congenital disorder of glycosylation 1t
Mus musculus (house mouse)
DOID:0081401
  • autosomal dominant distal hereditary motor neuronopathy 13
Mus musculus (house mouse)
DOID:0081320
  • multiple synostoses syndrome 4
Mus musculus (house mouse)
DOID:0111230
  • congenital muscular dystrophy-dystroglycanopathy type A11
  • Aliases:
    • MDDGA11
    • Walker-Warburg syndrome or muscle-eye-brain disease B3GALNT2-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A11
Mus musculus (house mouse)
DOID:0080918
  • polymicrogyria
Mus musculus (house mouse)
DOID:530
  • eyelid disease
Mus musculus (house mouse)
DOID:0080430
  • developmental and epileptic encephalopathy 65
  • Aliases:
    • DEE65
    • early infantile epileptic encephalopathy 65
Mus musculus (house mouse)
DOID:0050882
  • spinocerebellar ataxia type 5
Mus musculus (house mouse)
DOID:0080346
  • blepharocheilodontic syndrome 2
Mus musculus (house mouse)
DOID:0110317
  • hypertrophic cardiomyopathy 11
  • Aliases:
    • CMH11
    • cardiomyopathy familial hypertrophic 11
Mus musculus (house mouse)
DOID:0060404
  • chromosome 17q12 deletion syndrome
  • Aliases:
    • 17q12 microdeletion syndrome
Mus musculus (house mouse)
DOID:5223
  • infertility
Mus musculus (house mouse)
DOID:657
  • adenoma
  • Aliases:
    • acinar cell adenoma
    • acinic cell adenoma
    • adenomas
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