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 5251 - 5275 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism
DOID:0050565
  • autosomal recessive nonsyndromic deafness
Homo sapiens (human)
DOID:0050566
  • X-linked nonsyndromic deafness
  • Aliases:
    • X-linked deafness
Homo sapiens (human)
DOID:0050564
  • autosomal dominant nonsyndromic deafness
  • Aliases:
    • autosomal dominant deafness
Homo sapiens (human)
DOID:0110498
  • autosomal recessive nonsyndromic deafness 4
  • Aliases:
    • DFNB4
    • autosomal recessive deafness 4 with enlarged vestibular aqueduct
Homo sapiens (human)
DOID:0080571
  • congenital disorder of glycosylation Iu
  • Aliases:
    • congenital disorder of glycosylation 1u
Mus musculus (house mouse)
DOID:0080557
  • congenital disorder of glycosylation Ie
  • Aliases:
    • congenital disorder of glycosylation 1e
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:10579
  • leukodystrophy
Homo sapiens (human)
DOID:0111626
  • D-glyceric aciduria
  • Aliases:
    • D-glycerate kinase deficiency
    • D-glyceric acidemia
    • D-glycericacidemia
    • deficiency of glycerate kinase
    • non ketotic hyperglycinemia syndrome
Homo sapiens (human)
DOID:9268
  • glycine encephalopathy
  • Aliases:
    • Non-ketotic hyperglycinemia
    • nonketotic hyperglycinemia
Homo sapiens (human)
DOID:0112216
  • developmental and epileptic encephalopathy 80
  • Aliases:
    • DEE80
    • GPIBD20
    • early infantile epileptic encephalopathy 80
    • glycosylphosphatidylinositol biosynthesis defect 20
Caenorhabditis elegans
DOID:10112
  • sleeping sickness
  • Aliases:
    • African sleeping sickness
    • African trypanosomiasis
Caenorhabditis elegans
DOID:0110629
  • Wolfram syndrome 1
  • Aliases:
    • DIDMOAD
    • WFS1
    • diabetes mellitus AND insipidus with optic atrophy AND deafness
Homo sapiens (human)
DOID:10632
  • Wolfram syndrome
  • Aliases:
    • WFS
Homo sapiens (human)
DOID:0090054
  • episodic kinesigenic dyskinesia 2
Homo sapiens (human)
DOID:10646
  • schizotypal personality disorder
Homo sapiens (human)
DOID:0050158
  • desquamative interstitial pneumonia
  • Aliases:
    • RBILD
    • familial desquamative interstitial pneumonitis
    • respiratory bronchiolitis-associated interstitial lung disease
Homo sapiens (human)
DOID:9427
  • hypertensive encephalopathy
Homo sapiens (human)
DOID:0080169
  • tricuspid atresia
Homo sapiens (human)
DOID:8741
  • seborrheic dermatitis
  • Aliases:
    • SKIN SEBORRHEIC
    • Seborrhoeic dermatitis
    • Seborrhoeic eczema
    • seborrhea
Homo sapiens (human)
DOID:0060877
  • bullous congenital ichthyosiform erythroderma
  • Aliases:
    • bullous type ichthyosis
    • ichthyosis bullosa of Siemens
    • superficial epidermolytic ichthyosis
Homo sapiens (human)
DOID:2745
  • narcissistic personality disorder
Homo sapiens (human)
DOID:1509
  • avoidant personality disorder
  • Aliases:
    • anxious personality disorder
Homo sapiens (human)
DOID:12400
  • kleptomania
  • Aliases:
    • Pathological stealing
Homo sapiens (human)

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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