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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 3326 - 3350 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:0070376
  • developmental and epileptic encephalopathy 31B
  • Aliases:
    • DEE31B
Mus musculus (house mouse)
DOID:2975
  • cystic kidney disease
  • Aliases:
    • renal Cyst
Mus musculus (house mouse)
DOID:14717
  • centronuclear myopathy
  • Aliases:
    • myotubular myopathy
Mus musculus (house mouse)
DOID:0060558
  • lethal congenital contracture syndrome
Mus musculus (house mouse)
DOID:0050548
  • hereditary sensory neuropathy
  • Aliases:
    • familial dysautonomia, type II
    • hereditary sensory and autonomic neuropathy
Mus musculus (house mouse)
DOID:4926
  • bronchiolo-alveolar adenocarcinoma
  • Aliases:
    • Bronchioalveolar lung carcinoma
    • Bronchioloalveolar carcinoma
    • Minimally Invasive Lung Adenocarcinoma
Mus musculus (house mouse)
DOID:0070158
  • hereditary sensory neuropathy type 1E
  • Aliases:
    • HSN1E
    • hereditary sensory neuropathy type IE
Mus musculus (house mouse)
DOID:0050968
  • autosomal dominant cerebellar ataxia, deafness and narcolepsy
Mus musculus (house mouse)
DOID:8456
  • choline deficiency disease
  • Aliases:
    • choline deficiency
Mus musculus (house mouse)
DOID:288
  • endometriosis of uterus
  • Aliases:
    • Endometriosis interna
    • Endometriosis of myometrium
    • Endometriosis, myometrium
    • adenomyosis
    • uterine Adenomyosis
Mus musculus (house mouse)
DOID:0110676
  • congenital myasthenic syndrome 13
  • Aliases:
    • CMS13
    • CMSTA2
    • congenital myasthenic syndrome 13 with tubular aggregates
    • congenital myasthenic syndrome with tubular aggregates 2
Mus musculus (house mouse)
DOID:0080562
  • congenital disorder of glycosylation Ij
  • Aliases:
    • Congenital disorder of glycosylation 1j
Mus musculus (house mouse)
DOID:0080557
  • congenital disorder of glycosylation Ie
  • Aliases:
    • congenital disorder of glycosylation 1e
Mus musculus (house mouse)
DOID:0080571
  • congenital disorder of glycosylation Iu
  • Aliases:
    • congenital disorder of glycosylation 1u
Mus musculus (house mouse)
DOID:0080642
  • Middle East respiratory syndrome
Mus musculus (house mouse)
DOID:0070063
  • autosomal dominant intellectual developmental disorder 33
  • Aliases:
    • MRD33
    • autosomal dominant mental retardation 33
    • autosomal dominant non-syndromic intellectual disability 33
Mus musculus (house mouse)
DOID:13250
  • diarrhea
Mus musculus (house mouse)
DOID:0060296
  • congenital secretory chloride diarrhea 1
  • Aliases:
    • congenital chloride diarrhea finnish type
    • congenital chloride diarrhoea finnish type
    • congenital chloridorrhea
    • congenital secretory chloride diarrhoea 1
Mus musculus (house mouse)
DOID:3227
  • tracheal stenosis
  • Aliases:
    • Stenosis of trachea
Mus musculus (house mouse)
DOID:480
  • movement disease
Mus musculus (house mouse)
DOID:3602
  • toxic encephalopathy
  • Aliases:
    • neurotoxicity
    • neurotoxicity syndrome
Mus musculus (house mouse)
DOID:5425
  • ovarian hyperstimulation syndrome
  • Aliases:
    • secondary Meig's syndrome
Mus musculus (house mouse)
DOID:1742
  • drug psychosis
  • Aliases:
    • Drug-induced psychosis
    • Drug-induced psychotic disorder
Mus musculus (house mouse)
DOID:251
  • alcohol-induced mental disorder
Mus musculus (house mouse)
DOID:4990
  • essential tremor
  • Aliases:
    • benign essential tremor
    • essential hereditary tremor
    • shaky hand syndrome
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: December 9, 2024