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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 1626 - 1650 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:11716
  • prediabetes syndrome
  • Aliases:
    • Prediabetes
    • impaired glucose tolerance
    • prediabetic state
Mus musculus (house mouse)
DOID:13141
  • uveitis
Mus musculus (house mouse)
DOID:2326
  • gastroenteritis
  • Aliases:
    • cholera morbus
    • infectious colitis, enteritis and gastroenteritis
Mus musculus (house mouse)
DOID:0070352
  • stress-induced childhood-onset neurodegeneration with variable ataxia and seizures
  • Aliases:
    • CONDSIAS
Mus musculus (house mouse)
DOID:890
  • mitochondrial encephalomyopathy
Mus musculus (house mouse)
DOID:8515
  • Cor pulmonale
  • Aliases:
    • cardiopulmonary disease
    • pulmonary heart disease
Mus musculus (house mouse)
DOID:0050663
  • Bethlem myopathy
  • Aliases:
    • benign congenital muscular dystrophy
Mus musculus (house mouse)
DOID:1035
  • aggressive NK-cell leukemia
  • Aliases:
    • aggressive NK-cell leukaemia
    • large granular Lymphocyte Leukemia, NK-cell type
    • natural killer cell leukaemia
    • natural killer cell leukemia
Mus musculus (house mouse)
DOID:4483
  • rhinitis
Mus musculus (house mouse)
DOID:0050452
  • mevalonic aciduria
  • Aliases:
    • Mevalonate Kinase Deficiency
Mus musculus (house mouse)
DOID:5844
  • myocardial infarction
  • Aliases:
    • Myocardial infarct
    • heart attack
Mus musculus (house mouse)
DOID:0050156
  • idiopathic pulmonary fibrosis
  • Aliases:
    • FIBROCYSTIC PULMONARY DYSPLASIA
    • IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL
    • cryptogenic fibrosing alveolitis
Mus musculus (house mouse)
DOID:607
  • paraplegia
  • Aliases:
    • Paraplegia, lower
Mus musculus (house mouse)
DOID:5212
  • congenital disorder of glycosylation
  • Aliases:
    • carbohydrate-deficient glycoprotein syndrome
Mus musculus (house mouse)
DOID:0070218
  • familial hyperinsulinemic hypoglycemia 2
  • Aliases:
    • Autosomal recessive hyperinsulinemic hypoglycemia due to Kir6.2 deficiency
    • HHF2
    • hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia
Mus musculus (house mouse)
DOID:1561
  • cognitive disorder
  • Aliases:
    • cognitive disease
Mus musculus (house mouse)
DOID:12803
  • Sly syndrome
  • Aliases:
    • MPS VII - Sly syndrome
    • beta-glucuronidase deficiency
    • deficiency of beta-glucuronidase
    • mucopolysaccharidosis VII
Mus musculus (house mouse)
DOID:14330
  • Parkinson's disease
  • Aliases:
    • Parkinson disease
    • paralysis agitans
Mus musculus (house mouse)
DOID:0110858
  • polycystic kidney disease 1
  • Aliases:
    • Apkd1
    • Pkd1
    • Polycystic Kidney Disease, Adult, Type I
Mus musculus (house mouse)
DOID:0080119
  • mitochondrial DNA depletion syndrome 1
  • Aliases:
    • mitochondrial DNA depletion syndrome 1 (MNGIE type)
    • mitochondrial neurogastrointestinal encephalopathy syndrome, TYMP-related
Mus musculus (house mouse)
DOID:11121
  • pulpitis
  • Aliases:
    • pulp stones
Mus musculus (house mouse)
DOID:2526
  • prostate adenocarcinoma
Mus musculus (house mouse)
DOID:3213
  • demyelinating disease
  • Aliases:
    • demyelinating disorder
Mus musculus (house mouse)
DOID:13268
  • porphyria
  • Aliases:
    • Hematoporphyria
    • Porphyrinopathy
    • disorder of porphyrin and hem metabolism
    • disorder of porphyrin metabolism
Mus musculus (house mouse)
DOID:5394
  • prolactinoma
  • Aliases:
    • PITUITARY ADENOMA, PROLACTIN-SECRETING
    • Prolactinoma of Pituitary gland
    • familial prolactinoma
Mus musculus (house mouse)
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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