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 9551 - 9575 of 15957 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:0080245
  • Galloway-Mowat syndrome 3
Homo sapiens (human)
DOID:0080930
  • primary localized cutaneous amyloidosis 1
  • Aliases:
    • familial primary localized cutaneous amyloidosis-1
Homo sapiens (human)
DOID:612
  • primary immunodeficiency disease
  • Aliases:
    • hypoimmunity
    • immune deficiency disorder
    • immunodeficiency syndrome
Saccharomyces cerevisiae S288C
DOID:104
  • bacterial infectious disease
Saccharomyces cerevisiae S288C
DOID:0081183
  • autosomal recessive intellectual developmental disorder 7
Saccharomyces cerevisiae S288C
DOID:0111839
  • congenital disorder of glycosylation Icc
  • Aliases:
    • congenital disorder of glycosylation type Icc
Saccharomyces cerevisiae S288C
DOID:0080319
  • X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia
  • Aliases:
    • XMEN
Saccharomyces cerevisiae S288C
DOID:0110939
  • autosomal recessive osteopetrosis 5
  • Aliases:
    • OPTB5
    • infantile malignant osteopetrosis 3
Homo sapiens (human)
DOID:0110480
  • autosomal recessive nonsyndromic deafness 22
  • Aliases:
    • DFNB22
    • autosomal recessive deafness 22
Homo sapiens (human)
DOID:0110474
  • autosomal recessive nonsyndromic deafness 18B
  • Aliases:
    • DFNB18B
    • autosomal recessive deafness 18B
Homo sapiens (human)
DOID:0060394
  • chromosome 15q13.3 microdeletion syndrome
  • Aliases:
    • 15q13.3 microdeletion syndrome
Homo sapiens (human)
DOID:0080163
  • otulipenia
  • Aliases:
    • autoinflammation, panniculitis and dermatosis syndrome
    • otulin-related autoinflammatory syndrome
Homo sapiens (human)
DOID:9410
  • panhypopituitarism
  • Aliases:
    • Simmond's disease
    • Simmonds' disease
    • combined pituitary hormone deficiency
Homo sapiens (human)
DOID:0111806
  • syndromic microphthalmia 5
  • Aliases:
    • MCOPS5
    • syndromic microphthalmia type 5
    • syndromic microphthalmia/anophthalmia due to OTX2 mutation
Homo sapiens (human)
DOID:0070339
  • cerebellar hyplasia/atrophy, epilepsy, and global developmental delay
Homo sapiens (human)
DOID:2741
  • bilirubin metabolic disorder
  • Aliases:
    • hereditary hyperbilirubinemia
    • hyperbilirubinemia
Drosophila melanogaster (fruit fly)
DOID:12308
  • Dubin-Johnson syndrome
  • Aliases:
    • Dubin Johnson syndrome
    • chronic idiopathic jaundice
Drosophila melanogaster (fruit fly)
DOID:8866
  • actinic keratosis
  • Aliases:
    • SK - Solar keratosis
    • Senile hyperkeratosis
    • Solar keratosis
    • actinic (Solar) Keratosis
Mus musculus (house mouse)
DOID:8689
  • anorexia nervosa
Drosophila melanogaster (fruit fly)
DOID:0110429
  • dilated cardiomyopathy 1H
  • Aliases:
    • dilated cardiomyopathy with conduction defect
Drosophila melanogaster (fruit fly)
DOID:13189
  • gout
  • Aliases:
    • Articular gout
    • Gouty arthropathy
    • gouty arthritis
Drosophila melanogaster (fruit fly)
DOID:1070
  • primary open angle glaucoma
  • Aliases:
    • chronic simple glaucoma
Drosophila melanogaster (fruit fly)
DOID:13544
  • low tension glaucoma
  • Aliases:
    • Normal tension glaucoma
Drosophila melanogaster (fruit fly)
DOID:0060180
  • colitis
Drosophila melanogaster (fruit fly)
DOID:8893
  • psoriasis
Drosophila melanogaster (fruit fly)

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Last updated: December 9, 2024