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 7601 - 7625 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism
DOID:2741
  • bilirubin metabolic disorder
  • Aliases:
    • hereditary hyperbilirubinemia
    • hyperbilirubinemia
Saccharomyces cerevisiae S288C
DOID:3803
  • Crigler-Najjar syndrome
  • Aliases:
    • Bilirubin UDP glucuronyl transferase deficiency
    • Crigler Najjar syndrome
    • Crigler-Najjar syndrome, type I
Saccharomyces cerevisiae S288C
DOID:4988
  • alcoholic pancreatitis
Saccharomyces cerevisiae S288C
DOID:2739
  • Gilbert syndrome
  • Aliases:
    • Constitutional hyperbilirubinemia
    • Gilbert's disease
    • Gilbert's syndrome
    • Gilbert-Meulengracht syndrome
    • hereditary nonhemolytic jaundice
Saccharomyces cerevisiae S288C
DOID:10211
  • cholelithiasis
Saccharomyces cerevisiae S288C
DOID:8778
  • Crohn's disease
  • Aliases:
    • Crohn disease
    • Crohn's disease of colon
    • Crohn's disease of large bowel
    • Granulomatous Colitis
    • Pediatric Crohn's disease
Saccharomyces cerevisiae S288C
DOID:8692
  • myeloid leukemia
  • Aliases:
    • Non-Lymphocytic Leukemia
    • leukaemia myelogenous
    • leukemia myelogenous
    • myeloid granulocytic leukaemia
    • myeloid granulocytic leukemia
    • myeloid leukaemia
Saccharomyces cerevisiae S288C
DOID:653
  • purine-pyrimidine metabolic disorder
  • Aliases:
    • inborn errors of purine-pyrimidine metabolism
Saccharomyces cerevisiae S288C
DOID:5813
  • purine nucleoside phosphorylase deficiency
  • Aliases:
    • PNP deficiency
    • Purine-Nucleoside Phosphorylase deficiency
    • deficiency of inosine phosphorylase
Saccharomyces cerevisiae S288C
DOID:1574
  • alcohol use disorder
  • Aliases:
    • Ethanol abuse
    • alcohol abuse
Saccharomyces cerevisiae S288C
DOID:1826
  • epilepsy
  • Aliases:
    • epilepsy syndrome
    • epileptic syndrome
Saccharomyces cerevisiae S288C
DOID:1289
  • neurodegenerative disease
  • Aliases:
    • degenerative disease
Saccharomyces cerevisiae S288C
DOID:0111442
  • optic atrophy 9
  • Aliases:
    • OPA9
Saccharomyces cerevisiae S288C
DOID:1891
  • optic nerve disease
  • Aliases:
    • disorder of the second nerve
    • optic nerve disorder
    • optic neuropathy
Saccharomyces cerevisiae S288C
DOID:0050883
  • infantile cerebellar-retinal degeneration
Saccharomyces cerevisiae S288C
DOID:331
  • central nervous system disease
Saccharomyces cerevisiae S288C
DOID:2978
  • carbohydrate metabolic disorder
  • Aliases:
    • disorder of carbohydrate transport and metabolism
    • inborn carbohydrate metabolism disorder
    • inborn errors of carbohydrate metabolism
Saccharomyces cerevisiae S288C
DOID:5204
  • fructose-1,6-bisphosphatase deficiency
  • Aliases:
    • fructose 1 phosphate aldolase deficiency
    • fructose-1,6-diphosphatase deficiency
Saccharomyces cerevisiae S288C
DOID:0014667
  • disease of metabolism
  • Aliases:
    • metabolic disease
Saccharomyces cerevisiae S288C
DOID:0080208
  • metabolic dysfunction-associated steatotic liver disease
  • Aliases:
    • MAFLD
    • MASLD
    • NAFLD
    • metabolic dysfunction-associated fatty liver disease
    • metabolic dysfunction-related steatotic liver disease
    • metabolic-associated fatty liver disease
    • non-alcoholic fatty liver disease
    • nonalcoholic fatty liver disease
Saccharomyces cerevisiae S288C
DOID:0050453
  • lissencephaly
Saccharomyces cerevisiae S288C
DOID:0050560
  • Walker-Warburg syndrome
  • Aliases:
    • HARD syndrome
    • cerebroocular dysplasia-muscular dystrophy syndrome
Saccharomyces cerevisiae S288C
DOID:0112374
  • muscular dystrophy-dystroglycanopathy
  • Aliases:
    • MDDG
Saccharomyces cerevisiae S288C
DOID:9884
  • muscular dystrophy
Saccharomyces cerevisiae S288C
DOID:0112380
  • muscular dystrophy-dystroglycanopathy type B2
  • Aliases:
    • MDDGB2
    • congenital muscular dystrophy POMT2-related
Saccharomyces cerevisiae S288C

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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