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 2326 - 2350 of 4621 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:5690
  • well-differentiated liposarcoma
  • Aliases:
    • atypical lipomatous tumor
Homo sapiens (human)
DOID:5704
  • sclerosing liposarcoma
Homo sapiens (human)
DOID:0060402
  • chromosome 17p13.1 deletion syndrome
Homo sapiens (human)
DOID:74
  • hematopoietic system disease
  • Aliases:
    • Blood disease
    • Blood dyscrasia
    • DISEASE OF THE BLOOD AND BLOOD-FORMING ORGANS
    • Hematological disease
    • blood disorder
    • disease of haematopoietic system
    • disease of hematopoietic system
    • haematopoietic system disease
Homo sapiens (human)
DOID:674
  • cleft palate
  • Aliases:
    • Palatoschisis
Homo sapiens (human)
DOID:0110213
  • isolated cleft palate
Homo sapiens (human)
DOID:0050453
  • lissencephaly
Homo sapiens (human)
DOID:2717
  • Bloom syndrome
  • Aliases:
    • Bloom-Torre-Machacek syndrome
    • Congenital Telangiectatic Erythema syndrome
Homo sapiens (human)
DOID:0111344
  • myeloproliferative disorder with eosinophilia
  • Aliases:
    • chronic myeloproliferative disorder with eosinophilia
Homo sapiens (human)
DOID:0110915
  • childhood hypophosphatasia
Homo sapiens (human)
DOID:0111353
  • arthrogryposis, renal dysfunction, and cholestasis 1
  • Aliases:
    • ARCS1
Homo sapiens (human)
DOID:0050763
  • ARC syndrome
  • Aliases:
    • ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS
    • Arthrogryposis, renal dysfunction and cholestasis (ARC) syndrome
    • Arthrogryposis-renal dysfunction-cholestasis
Homo sapiens (human)
DOID:3308
  • embryonal carcinoma
  • Aliases:
    • primary extragonadal embryonal carcinoma
Homo sapiens (human)
DOID:12466
  • secondary hyperparathyroidism
Homo sapiens (human)
DOID:0070086
  • schizophrenia 10
  • Aliases:
    • SCZD10
Homo sapiens (human)
DOID:9498
  • pulmonary eosinophilia
Homo sapiens (human)
DOID:9503
  • Loeffler syndrome
  • Aliases:
    • Loeffler's pneumonia
    • Loffler's syndrome
Homo sapiens (human)
DOID:5870
  • eosinophilic pneumonia
  • Aliases:
    • Pneumonia, eosinophilic
Homo sapiens (human)
DOID:0110338
  • osteogenesis imperfecta type 17
  • Aliases:
    • OI17
    • osteogenesis imperfecta type XVII
Homo sapiens (human)
DOID:0110341
  • osteogenesis imperfecta type 2
  • Aliases:
    • OI2
    • Vrolik type of osteogenesis imperfecta
    • osteogenesis imperfecta type II
    • perinatal lethal osteogenesis imperfecta congenita
Homo sapiens (human)
DOID:0110336
  • osteogenesis imperfecta type 8
  • Aliases:
    • OI8
    • osteogenesis imperfecta type VIII
Homo sapiens (human)
DOID:0110346
  • osteogenesis imperfecta type 10
  • Aliases:
    • OI10
    • osteogenesis imperfecta type X
Homo sapiens (human)
DOID:0110342
  • osteogenesis imperfecta type 13
  • Aliases:
    • OI13
    • osteogenesis imperfecta type XIII
Homo sapiens (human)
DOID:0110348
  • osteogenesis imperfecta type 12
  • Aliases:
    • OI12
    • osteogenesis imperfecta type XII
Homo sapiens (human)
DOID:0110343
  • osteogenesis imperfecta type 14
  • Aliases:
    • OI14
    • osteogenesis imperfecta type XIV
Homo sapiens (human)

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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: August 19, 2024