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 4701 - 4725 of 7942 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism
DOID:14451
  • hyperkalemic periodic paralysis
  • Aliases:
    • familial hyperkalemic periodic paralysis
Homo sapiens (human)
DOID:14452
  • hypokalemic periodic paralysis
  • Aliases:
    • Hypokalemic familial periodic paralysis
    • Periodic paralysis I
    • Westphal disease
    • familial hypokalemic periodic paralysis
    • periodic hypokalemic paralysis
Homo sapiens (human)
DOID:14453
  • farmer's lung
  • Aliases:
    • Farmers lung
    • farmer lung
Mus musculus (house mouse)
DOID:14453
  • farmer's lung
  • Aliases:
    • Farmers lung
    • farmer lung
Homo sapiens (human)
DOID:14453
  • farmer's lung
  • Aliases:
    • Farmers lung
    • farmer lung
Rattus norvegicus (Norway rat)
DOID:14456
  • Brucella melitensis brucellosis
Homo sapiens (human)
DOID:14464
  • neuroleptic malignant syndrome
Homo sapiens (human)
DOID:14484
  • sporotrichosis
Homo sapiens (human)
DOID:14497
  • Wolman disease
  • Aliases:
    • Acid esterase deficiency
    • Acid lipase deficiency
    • Wolman xanthomatosis
    • Wolman's disease
    • Wolman's or triglyceride storage type III disease
    • Xanthomatosis, familial
    • acute infantile lysosomal acid lipase deficiency
    • complete LAL deficiency
    • complete LIPA deficiency
    • complete cholesterol ester hydrolase deficiency
    • complete lysosomal acid lipase deficiency
Mus musculus (house mouse)
DOID:14497
  • Wolman disease
  • Aliases:
    • Acid esterase deficiency
    • Acid lipase deficiency
    • Wolman xanthomatosis
    • Wolman's disease
    • Wolman's or triglyceride storage type III disease
    • Xanthomatosis, familial
    • acute infantile lysosomal acid lipase deficiency
    • complete LAL deficiency
    • complete LIPA deficiency
    • complete cholesterol ester hydrolase deficiency
    • complete lysosomal acid lipase deficiency
Homo sapiens (human)
DOID:14498
  • lipoid proteinosis
  • Aliases:
    • Lipid proteinosis
    • URBACH-WIETHE DISEASE
Homo sapiens (human)
DOID:14499
  • Fabry disease
  • Aliases:
    • Alpha-galactosidase A deficiency
    • Angiokeratoma Corporis Diffusum
    • Fabry Disease, Cardiac Variant
    • Fabry's disease
    • alpha galactosidase deficiency
    • deficiency of melibiase
Homo sapiens (human)
DOID:14499
  • Fabry disease
  • Aliases:
    • Alpha-galactosidase A deficiency
    • Angiokeratoma Corporis Diffusum
    • Fabry Disease, Cardiac Variant
    • Fabry's disease
    • alpha galactosidase deficiency
    • deficiency of melibiase
Mus musculus (house mouse)
DOID:14499
  • Fabry disease
  • Aliases:
    • Alpha-galactosidase A deficiency
    • Angiokeratoma Corporis Diffusum
    • Fabry Disease, Cardiac Variant
    • Fabry's disease
    • alpha galactosidase deficiency
    • deficiency of melibiase
Rattus norvegicus (Norway rat)
DOID:14500
  • fucosidosis
  • Aliases:
    • A-fucosidase deficiency
    • alpha fucosidase deficiency
Rattus norvegicus (Norway rat)
DOID:14500
  • fucosidosis
  • Aliases:
    • A-fucosidase deficiency
    • alpha fucosidase deficiency
Drosophila melanogaster (fruit fly)
DOID:14500
  • fucosidosis
  • Aliases:
    • A-fucosidase deficiency
    • alpha fucosidase deficiency
Homo sapiens (human)
DOID:14500
  • fucosidosis
  • Aliases:
    • A-fucosidase deficiency
    • alpha fucosidase deficiency
Caenorhabditis elegans
DOID:14500
  • fucosidosis
  • Aliases:
    • A-fucosidase deficiency
    • alpha fucosidase deficiency
Mus musculus (house mouse)
DOID:14501
  • Sjogren-Larsson syndrome
  • Aliases:
    • FALDH deficiency
    • SLS
    • Sjogren Larsson syndrome
    • Sjogren-Larsson's syndrome
    • fatty acid alcohol oxidoreductase deficiency
Homo sapiens (human)
DOID:14502
  • cholesterol ester storage disease
  • Aliases:
    • CESD
    • partial LAL deficiency
    • partial LIPA deficiency
    • partial cholesterol ester hydrolase deficiency
    • partial lysosomal acid lipase deficiency
Homo sapiens (human)
DOID:14502
  • cholesterol ester storage disease
  • Aliases:
    • CESD
    • partial LAL deficiency
    • partial LIPA deficiency
    • partial cholesterol ester hydrolase deficiency
    • partial lysosomal acid lipase deficiency
Mus musculus (house mouse)
DOID:14503
  • neuronal ceroid lipofuscinosis
  • Aliases:
    • hereditary ceroid lipofuscinosis
Homo sapiens (human)
DOID:14504
  • Niemann-Pick disease
  • Aliases:
    • Sphingomyelinase Deficiency Disease
    • lipoid histiocytosis
    • sphingomyelin lipidosis
Caenorhabditis elegans
DOID:14504
  • Niemann-Pick disease
  • Aliases:
    • Sphingomyelinase Deficiency Disease
    • lipoid histiocytosis
    • sphingomyelin lipidosis
Mus musculus (house mouse)

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Last updated: August 19, 2024