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 1176 - 1200 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism
DOID:10718
  • giardiasis
  • Aliases:
    • Infection by Giardia lamblia
    • beaver feaver
Homo sapiens (human)
DOID:10540
  • gastric lymphoma
  • Aliases:
    • Lymphoma of the stomach
Homo sapiens (human)
DOID:0050909
  • extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue
  • Aliases:
    • MALT lymphoma
    • MALT lymphoma of the dura
    • mucosa-associated lymphoid tissue lymphoma
Homo sapiens (human)
DOID:13271
  • cutaneous porphyria
  • Aliases:
    • Erythropoietic porphyria
Homo sapiens (human)
DOID:13270
  • erythropoietic protoporphyria
  • Aliases:
    • EPP
    • Protoporphyria
Homo sapiens (human)
DOID:8432
  • polycythemia
  • Aliases:
    • Erythrocythemia
Homo sapiens (human)
DOID:8997
  • polycythemia vera
  • Aliases:
    • Osler-Vaquez syndrome
    • Polycythaemia rubra vera
    • Proliferative polycythaemia
    • chronic erythremia
Homo sapiens (human)
DOID:3721
  • plasmacytoma
  • Aliases:
    • Myeloma - solitary
    • Myeloma, solitary
    • Solitary myeloma
    • Solitary plasmacytoma
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
Homo sapiens (human)
DOID:0080217
  • lysosomal acid lipase deficiency
  • Aliases:
    • LAL deficiency
    • LAL-D
Homo sapiens (human)
DOID:13316
  • exocrine pancreatic insufficiency
  • Aliases:
    • EPI
Homo sapiens (human)
DOID:1731
  • histoplasmosis
Homo sapiens (human)
DOID:8712
  • neurofibromatosis
Homo sapiens (human)
DOID:0050670
  • ataxic cerebral palsy
  • Aliases:
    • hypotonic cerebral palsy
Homo sapiens (human)
DOID:4798
  • aggressive systemic mastocytosis
  • Aliases:
    • ASM
    • Lymphadenopathic mastocytosis with eosinophilia
Homo sapiens (human)
DOID:350
  • mastocytosis
  • Aliases:
    • mast cell hyperplasia
Homo sapiens (human)
DOID:13317
  • hyperinsulinemic hypoglycemia
  • Aliases:
    • Islet cell hyperplasia
    • nesidioblastosis
    • persistent hyperinsulinemia hypoglycemia of infancy
Homo sapiens (human)
DOID:0070218
  • familial hyperinsulinemic hypoglycemia 2
  • Aliases:
    • Autosomal recessive hyperinsulinemic hypoglycemia due to Kir6.2 deficiency
    • HHF2
    • hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia
Homo sapiens (human)
DOID:0070219
  • familial hyperinsulinemic hypoglycemia 1
  • Aliases:
    • HHF1
Homo sapiens (human)
DOID:0111253
  • neurofibromatosis 1
  • Aliases:
    • NF1
    • Peripheral Neurofibromatosis
    • Recklinghausen's neurofibromatosis
    • neurofibromatosis type I
    • von Recklinghausen Disease
Homo sapiens (human)
DOID:0050524
  • maturity-onset diabetes of the young
  • Aliases:
    • MODY
    • Mason-type diabetes
Homo sapiens (human)
DOID:4660
  • indolent systemic mastocytosis
  • Aliases:
    • ISM
Homo sapiens (human)
DOID:349
  • systemic mastocytosis
  • Aliases:
    • SMCD - systemic mast cell disease
    • systemic tissue mast cell disease
Homo sapiens (human)
DOID:0080367
  • chronic eosinophilic leukemia
Homo sapiens (human)
DOID:2975
  • cystic kidney disease
  • Aliases:
    • renal Cyst
Homo sapiens (human)

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Last updated: August 19, 2024