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 5626 - 5650 of 7942 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism
DOID:0110342
  • osteogenesis imperfecta type 13
  • Aliases:
    • OI13
    • osteogenesis imperfecta type XIII
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: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:0110338
  • osteogenesis imperfecta type 17
  • Aliases:
    • OI17
    • osteogenesis imperfecta type XVII
Homo sapiens (human)
DOID:0110337
  • osteogenesis imperfecta type 7
  • Aliases:
    • OI7
    • osteogenesis imperfecta type VII
Homo sapiens (human)
DOID:0110336
  • osteogenesis imperfecta type 8
  • Aliases:
    • OI8
    • osteogenesis imperfecta type VIII
Homo sapiens (human)
DOID:0110335
  • osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures
Homo sapiens (human)
DOID:0110334
  • osteogenesis imperfecta type 1
  • Aliases:
    • OI1
    • osteogenesis imperfecta type I
Homo sapiens (human)
DOID:0110312
  • hypertrophic cardiomyopathy 6
  • Aliases:
    • CMH6
    • cardiomyopathy, familial hypertrophic 6
Homo sapiens (human)
DOID:0110312
  • hypertrophic cardiomyopathy 6
  • Aliases:
    • CMH6
    • cardiomyopathy, familial hypertrophic 6
Mus musculus (house mouse)
DOID:0110307
  • hypertrophic cardiomyopathy 1
  • Aliases:
    • CMH1
    • cardiomyopathy, familial hypertrophic 1
    • hypertrophic cardiomyopathy 19
Homo sapiens (human)
DOID:0110306
  • autosomal dominant limb-girdle muscular dystrophy type 3
  • Aliases:
    • LGMD1G
    • autosomal dominant limb-girdle muscular dystrophy type 1G
    • muscular dystrophy limb-girdle type 1G
Homo sapiens (human)
DOID:0110305
  • autosomal dominant limb-girdle muscular dystrophy type 1
  • Aliases:
    • LGMD1D
    • autosomal dominant limb-girdle muscular dystrophy type 1E
    • muscular dystrophy limb-girdle type 1D
    • muscular dystrophy limb-girdle type 1E
Homo sapiens (human)
DOID:0110304
  • autosomal dominant limb-girdle muscular dystrophy type 2
  • Aliases:
    • LGMD1F
    • autosomal dominant limb-girdle muscular dystrophy type 1F
    • muscular dystrophy limb-girdle type 1F
Homo sapiens (human)
DOID:0110303
  • autosomal dominant limb-girdle muscular dystrophy type 1H
  • Aliases:
    • LGMD1H
    • muscular dystrophy limb-girdle type 1H
Homo sapiens (human)
DOID:0110302
  • obsolete autosomal dominant limb-girdle muscular dystrophy type 1C
Homo sapiens (human)
DOID:0110301
  • obsolete autosomal dominant limb-girdle muscular dystrophy type 1B
Homo sapiens (human)
DOID:0110300
  • obsolete autosomal dominant limb-girdle muscular dystrophy type 1A
Homo sapiens (human)
DOID:0110299
  • autosomal recessive limb-girdle muscular dystrophy type 2I
  • Aliases:
    • LGMD2I
    • Limb-girdle muscular dystrophy due to FKRP deficiency
    • MDDGC5
    • muscular dystrophy limb-girdle type 2I
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C 5
    • muscular dystrophy-dystroglycanopathy limb-girdle FRKP-related
Rattus norvegicus (Norway rat)
DOID:0110299
  • autosomal recessive limb-girdle muscular dystrophy type 2I
  • Aliases:
    • LGMD2I
    • Limb-girdle muscular dystrophy due to FKRP deficiency
    • MDDGC5
    • muscular dystrophy limb-girdle type 2I
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C 5
    • muscular dystrophy-dystroglycanopathy limb-girdle FRKP-related
Xenopus tropicalis (tropical clawed frog)
DOID:0110299
  • autosomal recessive limb-girdle muscular dystrophy type 2I
  • Aliases:
    • LGMD2I
    • Limb-girdle muscular dystrophy due to FKRP deficiency
    • MDDGC5
    • muscular dystrophy limb-girdle type 2I
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C 5
    • muscular dystrophy-dystroglycanopathy limb-girdle FRKP-related
Xenopus laevis (African clawed frog)
DOID:0110299
  • autosomal recessive limb-girdle muscular dystrophy type 2I
  • Aliases:
    • LGMD2I
    • Limb-girdle muscular dystrophy due to FKRP deficiency
    • MDDGC5
    • muscular dystrophy limb-girdle type 2I
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C 5
    • muscular dystrophy-dystroglycanopathy limb-girdle FRKP-related
Mus musculus (house mouse)
DOID:0110299
  • autosomal recessive limb-girdle muscular dystrophy type 2I
  • Aliases:
    • LGMD2I
    • Limb-girdle muscular dystrophy due to FKRP deficiency
    • MDDGC5
    • muscular dystrophy limb-girdle type 2I
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C 5
    • muscular dystrophy-dystroglycanopathy limb-girdle FRKP-related
Danio rerio (zebrafish)
DOID:0110299
  • autosomal recessive limb-girdle muscular dystrophy type 2I
  • Aliases:
    • LGMD2I
    • Limb-girdle muscular dystrophy due to FKRP deficiency
    • MDDGC5
    • muscular dystrophy limb-girdle type 2I
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C 5
    • muscular dystrophy-dystroglycanopathy limb-girdle FRKP-related
Homo sapiens (human)

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