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 14576 - 14600 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:0060251
  • sclerosteosis
Rattus norvegicus (Norway rat)
DOID:0060756
  • sclerosteosis 1
  • Aliases:
    • SOST1
Rattus norvegicus (Norway rat)
DOID:0080036
  • SOST-related sclerosing bone dysplasia
  • Aliases:
    • van Buchem disease
Rattus norvegicus (Norway rat)
DOID:0080268
  • autosomal dominant nonsyndromic deafness 72
Homo sapiens (human)
DOID:0050948
  • autosomal dominant hypophosphatemic rickets
Homo sapiens (human)
DOID:2187
  • amelogenesis imperfecta
Mus musculus (house mouse)
DOID:10609
  • rickets
  • Aliases:
    • active rickets
Mus musculus (house mouse)
DOID:0080893
  • Bainbridge-Ropers syndrome
  • Aliases:
    • ASXL3-related disorder
Homo sapiens (human)
DOID:903
  • gastrointestinal lymphoma
Homo sapiens (human)
DOID:0050602
  • triple-A syndrome
  • Aliases:
    • AAAS
    • Achalasia-Addisonianism-Alacrimia syndrome
    • Allgrove Syndrome
Homo sapiens (human)
DOID:0081344
  • congenital myopathy 9B
Homo sapiens (human)
DOID:0081343
  • congenital myopathy 9A
Homo sapiens (human)
DOID:0081151
  • common variable immunodeficiency 8
  • Aliases:
    • common variable immunodeficiency-8 (CVID8) with autoimmunity
Mus musculus (house mouse)
DOID:0111813
  • syndactyly type 8
  • Aliases:
    • fusion of metacarpals 4 and 5
    • metacarpal 4-5 fusion
Mus musculus (house mouse)
DOID:1496
  • echinococcosis
  • Aliases:
    • Echinococcosis of liver
    • echinococcal disease
    • hepatic echinococcosis
    • hydatid disease
    • hydatidosis
    • liver echinococcus
    • pulmonary echinococcosis
Mus musculus (house mouse)
DOID:0111743
  • cerebellar ataxia type 47
  • Aliases:
    • SCA47
Mus musculus (house mouse)
DOID:0110513
  • autosomal recessive nonsyndromic deafness 61
  • Aliases:
    • DFNB61
    • autosomal recessive deafness 61
Mus musculus (house mouse)
DOID:0110639
  • congenital muscular dystrophy due to integrin alpha-7 deficiency
  • Aliases:
    • congenital muscular dystrophy with ITGA7 deficiency
    • congenital muscular dystrophy with integrin alpha-7 deficiency
    • congenital myopathy due to integrin alpha-7 deficiency
Rattus norvegicus (Norway rat)
DOID:0090102
  • autosomal dominant macrothrombocytopenia TUBB1-related
Homo sapiens (human)
DOID:0050921
  • pharynx squamous cell carcinoma
Homo sapiens (human)
DOID:11719
  • oculopharyngeal muscular dystrophy
  • Aliases:
    • Muscular dystrophy, oculopharyngeal
Homo sapiens (human)
DOID:0080960
  • amelogenesis imperfecta type 2A6
  • Aliases:
    • Amelogenesis imperfecta, hypomaturation type, IIA6
Homo sapiens (human)
DOID:0080448
  • developmental and epileptic encephalopathy 48
  • Aliases:
    • DEE48
    • early infantile epileptic encephalopathy 48
Homo sapiens (human)
DOID:0081423
  • familial focal epilepsy with variable foci 3
Homo sapiens (human)
DOID:0090068
  • giant axonal neuropathy 1
Homo sapiens (human)

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Last updated: December 9, 2024