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 1001 - 1025 of 4621 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism
DOID:4254
  • osteosclerosis
Homo sapiens (human)
DOID:3347
  • osteosarcoma
  • Aliases:
    • Osteogenic sarcoma
    • Skeletal sarcoma
    • bone tissue neoplasm
    • osteoid sarcoma
Homo sapiens (human)
DOID:0060849
  • osteoporosis-pseudoglioma syndrome
  • Aliases:
    • OPPG
    • ocular form of osteogenesis imperfecta
Homo sapiens (human)
DOID:11476
  • osteoporosis
Homo sapiens (human)
DOID:11991
  • osteopoikilosis
Homo sapiens (human)
DOID:13533
  • osteopetrosis
  • Aliases:
    • Albers-Schonberg disease
    • marble bone
Homo sapiens (human)
DOID:10159
  • osteonecrosis
  • Aliases:
    • Avascular necrosis of bone
    • aseptic necrosis
    • bone necrosis
Homo sapiens (human)
DOID:1019
  • osteomyelitis
Homo sapiens (human)
DOID:10573
  • osteomalacia
Homo sapiens (human)
DOID:0111532
  • osteoglophonic dysplasia
  • Aliases:
    • Fairbank-Keats syndrome
    • OGD
    • osteoglophonic dwarfism
Homo sapiens (human)
DOID:12347
  • osteogenesis imperfecta
  • Aliases:
    • Lobstein's syndrome
    • Osteopsathyrosis
    • Vrolik's disease
    • brittle bone disease
Homo sapiens (human)
DOID:0110335
  • osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures
Homo sapiens (human)
DOID:0110349
  • osteogenesis imperfecta type 9
  • Aliases:
    • OI9
    • osteogenesis imperfecta type IX
Homo sapiens (human)
DOID:0110336
  • osteogenesis imperfecta type 8
  • Aliases:
    • OI8
    • osteogenesis imperfecta type VIII
Homo sapiens (human)
DOID:0110337
  • osteogenesis imperfecta type 7
  • Aliases:
    • OI7
    • osteogenesis imperfecta type VII
Homo sapiens (human)
DOID:0110350
  • osteogenesis imperfecta type 6
  • Aliases:
    • OI6
    • osteogenesis imperfecta type VI
Homo sapiens (human)
DOID:0110344
  • osteogenesis imperfecta type 5
  • Aliases:
    • OI5
    • osteogenesis imperfecta type V
Homo sapiens (human)
DOID:0110340
  • osteogenesis imperfecta type 4
  • Aliases:
    • OI4
    • osteogenesis imperfecta type IV
    • osteogenesis imperfecta with normal sclera
Homo sapiens (human)
DOID:0110339
  • osteogenesis imperfecta type 3
  • Aliases:
    • OI3
    • osteogenesis imperfecta type III
    • progressively deforming osteogenesis imperfecta with normal sclera
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:0110338
  • osteogenesis imperfecta type 17
  • Aliases:
    • OI17
    • osteogenesis imperfecta type XVII
Homo sapiens (human)
DOID:0110345
  • osteogenesis imperfecta type 16
  • Aliases:
    • OI16
    • chromosome 11p11.2 deletion syndrome 91.3-KB
    • osteogenesis imperfecta type XVI
Homo sapiens (human)
DOID:0110347
  • osteogenesis imperfecta type 15
  • Aliases:
    • OI15
    • osteogenesis imperfecta type XV
Homo sapiens (human)
DOID:0110343
  • osteogenesis imperfecta type 14
  • Aliases:
    • OI14
    • osteogenesis imperfecta type XIV
Homo sapiens (human)
DOID:0110342
  • osteogenesis imperfecta type 13
  • Aliases:
    • OI13
    • osteogenesis imperfecta type XIII
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