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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 10276 - 10300 of 15957 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:12935
  • alcoholic cardiomyopathy
  • Aliases:
    • Alcohol-induced heart muscle disease
    • Dilated cardiomyopathy secondary to alcohol
Mus musculus (house mouse)
DOID:0070204
  • familial partial lipodystrophy type 3
  • Aliases:
    • FPLD3
    • PPARG-related FPLD
    • PPARG-related familial partial lipodystrophy
    • familial partial lipodystrophy associated with PPARG mutations
Mus musculus (house mouse)
DOID:11613
  • hyperandrogenism
  • Aliases:
    • hyperandrogenization syndrome
Rattus norvegicus (Norway rat)
DOID:0070204
  • familial partial lipodystrophy type 3
  • Aliases:
    • FPLD3
    • PPARG-related FPLD
    • PPARG-related familial partial lipodystrophy
    • familial partial lipodystrophy associated with PPARG mutations
Rattus norvegicus (Norway rat)
DOID:1907
  • malignant fibrous histiocytoma
  • Aliases:
    • Fibroxanthosarcoma
    • MFH
Mus musculus (house mouse)
DOID:1907
  • malignant fibrous histiocytoma
  • Aliases:
    • Fibroxanthosarcoma
    • MFH
Rattus norvegicus (Norway rat)
DOID:12506
  • Bell's palsy
  • Aliases:
    • Bell palsy
    • Bell's (facial) palsy
Rattus norvegicus (Norway rat)
DOID:12506
  • Bell's palsy
  • Aliases:
    • Bell palsy
    • Bell's (facial) palsy
Mus musculus (house mouse)
DOID:0110349
  • osteogenesis imperfecta type 9
  • Aliases:
    • OI9
    • osteogenesis imperfecta type IX
Mus musculus (house mouse)
DOID:0080693
  • Noonan syndrome-like disorder with loose anagen hair 2
Mus musculus (house mouse)
DOID:0080693
  • Noonan syndrome-like disorder with loose anagen hair 2
Rattus norvegicus (Norway rat)
DOID:0050962
  • spinocerebellar ataxia type 12
Mus musculus (house mouse)
DOID:0080472
  • developmental and epileptic encephalopathy 91
  • Aliases:
    • infantile or early childhood epileptic encephalopathy 1
Mus musculus (house mouse)
DOID:0110721
  • neuronal ceroid lipofuscinosis 1
  • Aliases:
    • CLN1
    • neuronal ceroid lipofuscinosis 1 variable age of onset
Rattus norvegicus (Norway rat)
DOID:14503
  • neuronal ceroid lipofuscinosis
  • Aliases:
    • hereditary ceroid lipofuscinosis
Drosophila melanogaster (fruit fly)
DOID:0110721
  • neuronal ceroid lipofuscinosis 1
  • Aliases:
    • CLN1
    • neuronal ceroid lipofuscinosis 1 variable age of onset
Drosophila melanogaster (fruit fly)
DOID:0110731
  • neuronal ceroid lipofuscinosis 3
  • Aliases:
    • Batten disease
    • CLN3
    • juvenile neuronal ceroid lipofuscinosis
Drosophila melanogaster (fruit fly)
DOID:0050715
  • methylmalonic aciduria and homocystinuria type cblC
  • Aliases:
    • Cobalamin C deficiency
    • MAHCC
Mus musculus (house mouse)
DOID:0070413
  • autosomal recessive spinocerebellar ataxia 32
  • Aliases:
    • SCAR32
Mus musculus (house mouse)
DOID:0070413
  • autosomal recessive spinocerebellar ataxia 32
  • Aliases:
    • SCAR32
Rattus norvegicus (Norway rat)
DOID:0110922
  • familial hemophagocytic lymphohistiocytosis 2
  • Aliases:
    • FHL2
    • HLH2
    • HPLH2
Mus musculus (house mouse)
DOID:4330
  • non-Langerhans-cell histiocytosis
Mus musculus (house mouse)
DOID:1725
  • peritoneum cancer
Rattus norvegicus (Norway rat)
DOID:1787
  • pericarditis
Mus musculus (house mouse)
DOID:0090127
  • camptodactyly-arthropathy-coxa vara-pericarditis syndrome
  • Aliases:
    • CACP
    • CACP syndrome
    • CAP syndrome
    • Jacobs syndrome
    • PAC syndrome
    • arthropathy-camptodactyly syndrome
    • camptodactyly-arthropathy-pericarditis syndrome
    • congenital familial hypertrophic synovitis
    • familial fibrosing serositis
    • pericarditis-arthropathy-camptodactyly syndrome
Mus musculus (house mouse)
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Last updated: December 9, 2024