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 3326 - 3350 of 4621 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism
DOID:12237
  • bile reflux
Homo sapiens (human)
DOID:4138
  • bile duct disease
  • Aliases:
    • bile duct disorder
    • disorder of bile duct
Homo sapiens (human)
DOID:4897
  • bile duct carcinoma
Homo sapiens (human)
DOID:4606
  • bile duct cancer
  • Aliases:
    • Ca extrahepatic bile ducts
    • bile duct tumor
    • malignant neoplasm of the extrahepatic bile duct
Homo sapiens (human)
DOID:5381
  • bile duct adenoma
  • Aliases:
    • Cholangioadenoma
Homo sapiens (human)
DOID:4896
  • bile duct adenocarcinoma
Homo sapiens (human)
DOID:0080200
  • bilateral renal aplasia
Homo sapiens (human)
DOID:0080923
  • bilateral parasagittal parieto-occipital polymicrogyria
  • Aliases:
    • bilateral temporooccipital polymicrogyria
Homo sapiens (human)
DOID:0111531
  • bilateral optic nerve hypoplasia
  • Aliases:
    • ONH
    • familial bilateral optic nerve hypoplasia
    • isolated optic nerve hypoplasia/aplasia
Homo sapiens (human)
DOID:6741
  • bilateral breast cancer
  • Aliases:
    • Bilateral breast carcinoma
Homo sapiens (human)
DOID:0080332
  • bicuspid aortic valve disease
  • Aliases:
    • Familial bicuspid aortic valve
Homo sapiens (human)
DOID:3633
  • beta-mannosidosis
  • Aliases:
    • Beta-D-mannosidosis
    • beta-mannosidase deficiency
    • lysosomal beta-mannosidase deficiency
Homo sapiens (human)
DOID:14723
  • beta-ketothiolase deficiency
  • Aliases:
    • 2-methyl-3-hydroxybutyricacidemia
    • 3-ketothiolase deficiency
    • 3-oxothiolase deficiency
    • Mitochondrial acetoacetyl-CoA Thiolase deficiency
    • alpha-methylacetoaceticaciduria
    • peroxisomal thiolase deficiency
Homo sapiens (human)
DOID:12241
  • beta thalassemia
Homo sapiens (human)
DOID:0050662
  • bestrophinopathy
  • Aliases:
    • autosomal recessive bestrophinopathy
Homo sapiens (human)
DOID:10322
  • berylliosis
  • Aliases:
    • beryllium poisoning
Homo sapiens (human)
DOID:13725
  • beriberi
Homo sapiens (human)
DOID:0070230
  • benign recurrent intrahepatic cholestasis
  • Aliases:
    • BRIC
    • Summerskill-Walshe-Tygstrup syndrome
Homo sapiens (human)
DOID:5157
  • benign pleural mesothelioma
  • Aliases:
    • Mesothelioma of Pleura
Homo sapiens (human)
DOID:1789
  • benign peritoneal mesothelioma
  • Aliases:
    • Mesothelioma of Peritoneum
Homo sapiens (human)
DOID:14264
  • benign neonatal seizures
  • Aliases:
    • benign familial neonatal seizures
    • benign neonatal convulsions
Homo sapiens (human)
DOID:2645
  • benign mesothelioma
  • Aliases:
    • benign tumor of Mesothelium
Homo sapiens (human)
DOID:4587
  • benign meningioma
  • Aliases:
    • meningioma, benign
Homo sapiens (human)
DOID:4658
  • benign mastocytoma
Homo sapiens (human)
DOID:5884
  • benign intermediate mesothelioma
  • Aliases:
    • Well-differentiated Papillary tumor of Mesothelium
Homo sapiens (human)

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024