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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 12826 - 12850 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:0080728
  • Ehlers-Danlos syndrome arthrochalasia type 2
Mus musculus (house mouse)
DOID:0080730
  • Ehlers-Danlos syndrome cardiac valvular type
Mus musculus (house mouse)
DOID:0080727
  • Ehlers-Danlos syndrome arthrochalasia type 1
Mus musculus (house mouse)
DOID:4257
  • Caffey disease
  • Aliases:
    • cortical congenital hyperostosis
    • infantile cortical hyperostosis
Mus musculus (house mouse)
DOID:0110334
  • osteogenesis imperfecta type 1
  • Aliases:
    • OI1
    • osteogenesis imperfecta type I
Mus musculus (house mouse)
DOID:4154
  • dentinogenesis imperfecta
Mus musculus (house mouse)
DOID:3507
  • dermatofibrosarcoma protuberans
Mus musculus (house mouse)
DOID:916
  • liver benign neoplasm
  • Aliases:
    • epithelial hepatic and intrahepatic bile duct neoplasm
Mus musculus (house mouse)
DOID:12241
  • beta thalassemia
Mus musculus (house mouse)
DOID:1474
  • aggressive periodontitis
  • Aliases:
    • juvenile periodontitis
Mus musculus (house mouse)
DOID:0110339
  • osteogenesis imperfecta type 3
  • Aliases:
    • OI3
    • osteogenesis imperfecta type III
    • progressively deforming osteogenesis imperfecta with normal sclera
Mus musculus (house mouse)
DOID:0110340
  • osteogenesis imperfecta type 4
  • Aliases:
    • OI4
    • osteogenesis imperfecta type IV
    • osteogenesis imperfecta with normal sclera
Mus musculus (house mouse)
DOID:0110341
  • osteogenesis imperfecta type 2
  • Aliases:
    • OI2
    • Vrolik type of osteogenesis imperfecta
    • osteogenesis imperfecta type II
    • perinatal lethal osteogenesis imperfecta congenita
Mus musculus (house mouse)
DOID:0112314
  • brain small vessel disease 2
  • Aliases:
    • BSVD2
    • porencephaly 2
Homo sapiens (human)
DOID:13129
  • severe pre-eclampsia
  • Aliases:
    • Severe pre-eclampsia, with delivery
    • antepartum severe pre-eclampsia
    • postpartum severe pre-eclampsia
    • severe preeclampsia
Homo sapiens (human)
DOID:0111345
  • transient bullous dermolysis of the newborn
  • Aliases:
    • DEB, bullous dermolysis of the newborn
    • DEB-BDN
Mus musculus (house mouse)
DOID:0111347
  • epidermolysis bullosa with congenital localized absence of skin and deformity of nails
  • Aliases:
    • EBD, Bart type
    • epidermolysis bullosa dystrophica, Bart type
Mus musculus (house mouse)
DOID:0080224
  • autosomal dominant dystrophic epidermolysis bullosa
Mus musculus (house mouse)
DOID:0080988
  • pretibial dystrophic epidermolysis bullosa
Mus musculus (house mouse)
DOID:0080086
  • nonsyndromic congenital nail disorder 8
  • Aliases:
    • isolated toenail dystrophy
Mus musculus (house mouse)
DOID:0060642
  • recessive dystrophic epidermolysis bullosa
  • Aliases:
    • RDEB, Hallopeau-Siemens type
    • autosomal recessive dystrophic epidermolysis bullosa generalisata gravis
    • autosomal recessive dystrophic epidermolysis bullosa, Hallopeau-Siemens type
Mus musculus (house mouse)
DOID:4959
  • epidermolysis bullosa dystrophica
  • Aliases:
    • Dystrophic epidermolysis bullosa
Mus musculus (house mouse)
DOID:0090050
  • dystonia 27
Mus musculus (house mouse)
DOID:2033
  • communication disorder
Mus musculus (house mouse)
DOID:0050558
  • Ullrich congenital muscular dystrophy
  • Aliases:
    • ULLRICH DISEASE
    • Ullrich scleroatonic muscular dystrophy
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: December 9, 2024