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 5676 - 5700 of 7942 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:1702
  • ichthyosis vulgaris
  • Aliases:
    • Dominant congenital ichthyosiform erythroderma
Homo sapiens (human)
DOID:4603
  • epidermolytic hyperkeratosis
  • Aliases:
    • Bullous ichthyosiform erythroderma
    • Epidermolytic palmoplantar hyperkeratosis
    • epidermolytic ichthyosis
Homo sapiens (human)
DOID:4535
  • hypotrichosis
Homo sapiens (human)
DOID:1570
  • ectropion
  • Aliases:
    • Ectropion of eyelid
    • Everted margin
Homo sapiens (human)
DOID:0050428
  • nonepidermolytic palmoplantar keratoderma
  • Aliases:
    • Thost-Unna Syndrome
    • Unna-Thost Syndrome
    • diffuse nonepidermolytic palmomplantar keratoderma
    • tylosis
Homo sapiens (human)
DOID:3390
  • palmoplantar keratosis
  • Aliases:
    • Keratosis palmaris et plantaris
    • Palmoplantar Keratoderma
    • palmo-plantar keratodermas
Homo sapiens (human)
DOID:11155
  • hypohidrosis
  • Aliases:
    • Oligohidrosis
Homo sapiens (human)
DOID:11156
  • anhidrosis
  • Aliases:
    • Adiaphoresis
    • absence of sweating
Homo sapiens (human)
DOID:0060713
  • autosomal recessive congenital ichthyosis 4B
  • Aliases:
    • ARCI4B
    • harlequin ichthyosis
    • harlequin type ichthyosis congenita
    • harlequin type ichthyosis fetalis
Homo sapiens (human)
DOID:9368
  • keratoconjunctivitis
Homo sapiens (human)
DOID:4677
  • keratitis
Homo sapiens (human)
DOID:13336
  • congenital toxoplasmosis
  • Aliases:
    • Toxoplasmosis - congen.
Homo sapiens (human)
DOID:0111005
  • cone-rod dystrophy 2
  • Aliases:
    • CORD2
    • CRD2
    • RCRD2
    • cone-rod retinal dystrophy 2
    • retinal cone-rod dystrophy 2
Homo sapiens (human)
DOID:0050661
  • vitelliform macular dystrophy
  • Aliases:
    • Best disease
    • Best macular dystrophy
    • juvenile-onset vitelliform macular dystrophy
Homo sapiens (human)
DOID:0080564
  • congenital disorder of glycosylation Il
  • Aliases:
    • congenital disorder of glycosylation 1l
Saccharomyces cerevisiae S288C
DOID:3312
  • bipolar disorder
  • Aliases:
    • Manic Bipolar Affective disorder
    • Manic Depressive disorder
    • Manic bipolar I disorder
    • bipolar depression
    • bipolar disorder manic phase
    • manic depression
    • manic disorder
    • mixed bipolar disorder
Saccharomyces cerevisiae S288C
DOID:11119
  • Gilles de la Tourette syndrome
  • Aliases:
    • Guinon's disease
    • Psychogenic tics
    • Tourette syndrome
    • motor-verbal tic disorder
Homo sapiens (human)
DOID:0080564
  • congenital disorder of glycosylation Il
  • Aliases:
    • congenital disorder of glycosylation 1l
Homo sapiens (human)
DOID:0080560
  • congenital disorder of glycosylation Ih
  • Aliases:
    • congenital disorder of glycosylation 1h
Saccharomyces cerevisiae S288C
DOID:0050770
  • polycystic liver disease
  • Aliases:
    • congenital cystic liver disease
    • congenital hepatic cyst
    • fibrocystic liver disease
Saccharomyces cerevisiae S288C
DOID:0080560
  • congenital disorder of glycosylation Ih
  • Aliases:
    • congenital disorder of glycosylation 1h
Homo sapiens (human)
DOID:4976
  • elephantiasis
Homo sapiens (human)
DOID:9621
  • non-congenital cyst of kidney
Homo sapiens (human)
DOID:10611
  • protein-losing enteropathy
  • Aliases:
    • Enteropathy, exudative
    • Exudative enteropathy
Homo sapiens (human)
DOID:0050770
  • polycystic liver disease
  • Aliases:
    • congenital cystic liver disease
    • congenital hepatic cyst
    • fibrocystic liver disease
Homo sapiens (human)

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Last updated: August 19, 2024