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 3651 - 3675 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism
DOID:10605
  • short bowel syndrome
  • Aliases:
    • acquired short bowel syndrome
    • short gut syndrome
Mus musculus (house mouse)
DOID:4483
  • rhinitis
Mus musculus (house mouse)
DOID:0060611
  • abdominal obesity-metabolic syndrome
Mus musculus (house mouse)
DOID:14018
  • alcoholic liver cirrhosis
  • Aliases:
    • Alcoholic Cirrhosis
    • Alcoholic cirrhosis of liver
    • Laennec's cirrhosis
    • Laennec's cirrhosis, alcoholic
    • Portal cirrhosis
Mus musculus (house mouse)
DOID:11394
  • adult respiratory distress syndrome
  • Aliases:
    • ARDS
    • Non-cardiogenic pulmonary edema
    • Shock lung
    • acute respiratory distress syndrome
    • adult RDS
Mus musculus (house mouse)
DOID:1924
  • hypogonadism
Mus musculus (house mouse)
DOID:2913
  • acute pancreatitis
Mus musculus (house mouse)
DOID:14221
  • abdominal obesity-metabolic syndrome 1
  • Aliases:
    • dysmetabolic syndrome X
    • metabolic syndrome X
Mus musculus (house mouse)
DOID:0111334
  • congenital leptin deficiency
  • Aliases:
    • LEPD
    • leptin deficiency or dysfunction
    • obesity due to congenital leptin deficiency
Mus musculus (house mouse)
DOID:0050855
  • renal fibrosis
Mus musculus (house mouse)
DOID:526
  • human immunodeficiency virus infectious disease
  • Aliases:
    • HIV infection
Mus musculus (house mouse)
DOID:9775
  • diastolic heart failure
Mus musculus (house mouse)
DOID:0112361
  • spondylocostal dysostosis 3
  • Aliases:
    • SCDO3
    • autosomal recessive spondylocostal dysostosis 3
Mus musculus (house mouse)
DOID:14502
  • cholesterol ester storage disease
  • Aliases:
    • CESD
    • partial LAL deficiency
    • partial LIPA deficiency
    • partial cholesterol ester hydrolase deficiency
    • partial lysosomal acid lipase deficiency
Mus musculus (house mouse)
DOID:14497
  • Wolman disease
  • Aliases:
    • Acid esterase deficiency
    • Acid lipase deficiency
    • Wolman xanthomatosis
    • Wolman's disease
    • Wolman's or triglyceride storage type III disease
    • Xanthomatosis, familial
    • acute infantile lysosomal acid lipase deficiency
    • complete LAL deficiency
    • complete LIPA deficiency
    • complete cholesterol ester hydrolase deficiency
    • complete lysosomal acid lipase deficiency
Mus musculus (house mouse)
DOID:0080217
  • lysosomal acid lipase deficiency
  • Aliases:
    • LAL deficiency
    • LAL-D
Mus musculus (house mouse)
DOID:0050563
  • nonsyndromic deafness
  • Aliases:
    • nonsyndromic hearing loss
    • nonsyndromic hereditary hearing loss
Mus musculus (house mouse)
DOID:10159
  • osteonecrosis
  • Aliases:
    • Avascular necrosis of bone
    • aseptic necrosis
    • bone necrosis
Mus musculus (house mouse)
DOID:971
  • tendinitis
Mus musculus (house mouse)
DOID:898
  • autosomal dominant polycystic kidney disease
  • Aliases:
    • ADPKD
    • Congenital biliary ectasias
    • POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1
Mus musculus (house mouse)
DOID:0111411
  • exudative vitreoretinopathy 4
  • Aliases:
    • EVR4
Mus musculus (house mouse)
DOID:10629
  • microphthalmia
  • Aliases:
    • microphthalmos
    • simple microphthalmos
Mus musculus (house mouse)
DOID:12559
  • idiopathic juvenile osteoporosis
  • Aliases:
    • Idiopathic osteoporosis
    • juvenile osteoporosis
Mus musculus (house mouse)
DOID:9719
  • neovascular inflammatory vitreoretinopathy
  • Aliases:
    • ADNIV
    • Retinitis proliferans
    • autosomal dominant neovascular inflammatory vitreoretinopathy
    • proliferative vitreoretinopathy
Mus musculus (house mouse)
DOID:0110937
  • autosomal dominant osteopetrosis 1
  • Aliases:
    • OPTA1
    • autosomal dominant osteopetrosis type 1
Mus musculus (house mouse)

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

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