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 6226 - 6250 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:0111100
  • maturity-onset diabetes of the young type 2
  • Aliases:
    • MODY glucokinase-related
    • MODY type 2
    • MODY2
Mus musculus (house mouse)
DOID:0111042
  • glycogen storage disease IXa
  • Aliases:
    • GSD type 9A
    • GSD type IXa
    • GSD9A
    • glycogen storage disease type 9A
    • glycogen storage disease type IXa
    • glycogenosis type 9A
    • glycogenosis type IXa
Mus musculus (house mouse)
DOID:12449
  • aplastic anemia
Mus musculus (house mouse)
DOID:479
  • angiokeratoma
  • Aliases:
    • Angiokeratoma of skin
    • Cutaneous Angiokeratoma
    • skin angiokeratoma
Mus musculus (house mouse)
DOID:5614
  • eye disease
Mus musculus (house mouse)
DOID:0050570
  • congenital disorder of glycosylation type I
Mus musculus (house mouse)
DOID:4029
  • gastritis
  • Aliases:
    • Erosive Gastritis
    • Erosive gastropathy
    • acute gastric mucosal erosion
Mus musculus (house mouse)
DOID:2739
  • Gilbert syndrome
  • Aliases:
    • Constitutional hyperbilirubinemia
    • Gilbert's disease
    • Gilbert's syndrome
    • Gilbert-Meulengracht syndrome
    • hereditary nonhemolytic jaundice
Mus musculus (house mouse)
DOID:0110637
  • muscular dystrophy-dystroglycanopathy type B6
  • Aliases:
    • MDC1D
    • MDDGB6
    • congenital muscular dystrophy LARGE-related
    • congenital muscular dystrophy type 1D
    • muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6
    • muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 6
Mus musculus (house mouse)
DOID:4500
  • hypokalemia
  • Aliases:
    • hypopotassemia
    • potassium deficiency disorder
Mus musculus (house mouse)
DOID:14227
  • azoospermia
Mus musculus (house mouse)
DOID:4926
  • bronchiolo-alveolar adenocarcinoma
  • Aliases:
    • Bronchioalveolar lung carcinoma
    • Bronchioloalveolar carcinoma
    • Minimally Invasive Lung Adenocarcinoma
Mus musculus (house mouse)
DOID:0050557
  • congenital muscular dystrophy
Mus musculus (house mouse)
DOID:4977
  • lymphedema
  • Aliases:
    • Lymphatic edema
    • Lymphoedema
Mus musculus (house mouse)
DOID:4194
  • glucose metabolism disease
  • Aliases:
    • disorder of glucose metabolism
Mus musculus (house mouse)
DOID:0060713
  • autosomal recessive congenital ichthyosis 4B
  • Aliases:
    • ARCI4B
    • harlequin ichthyosis
    • harlequin type ichthyosis congenita
    • harlequin type ichthyosis fetalis
Mus musculus (house mouse)
DOID:9409
  • diabetes insipidus
Mus musculus (house mouse)
DOID:12365
  • malaria
  • Aliases:
    • induced malaria
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:0111239
  • congenital muscular dystrophy-dystroglycanopathy type A10
  • Aliases:
    • MDDGA10
    • Walker-Warburg syndrome or muscle-eye-brain disease, TMEM5-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A10
Mus musculus (house mouse)
DOID:841
  • extrinsic allergic alveolitis
  • Aliases:
    • alveolitis
    • hypersensitivity pneumonitis
Mus musculus (house mouse)
DOID:8719
  • in situ carcinoma
Mus musculus (house mouse)
DOID:4762
  • vasculogenic impotence
Mus musculus (house mouse)
DOID:5154
  • borna disease
  • Aliases:
    • Enzootic encephalomyelitis
Mus musculus (house mouse)
DOID:2738
  • pseudoxanthoma elasticum
  • Aliases:
    • Gronblad-Strandberg syndrome
Mus musculus (house mouse)

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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