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 12476 - 12500 of 15957 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:5485
  • synovial sarcoma
Drosophila melanogaster (fruit fly)
DOID:0111862
  • congenital bilateral absence of vas deferens
  • Aliases:
    • CAVD
    • CBAVD
    • congenital bilateral agenesis of vas deferens
    • congenital bilateral aplasia of vas deferens
Homo sapiens (human)
DOID:5733
  • salpingitis
Homo sapiens (human)
DOID:0111864
  • autosomal recessive congenital bilateral absence of vas deferens
Homo sapiens (human)
DOID:13316
  • exocrine pancreatic insufficiency
  • Aliases:
    • EPI
Homo sapiens (human)
DOID:693
  • dental enamel hypoplasia
  • Aliases:
    • enamel hypoplasia
Homo sapiens (human)
DOID:0080526
  • bronchiectasis 1
Homo sapiens (human)
DOID:9563
  • bronchiectasis
  • Aliases:
    • Polynesian bronchiectasis
Homo sapiens (human)
DOID:13166
  • allergic bronchopulmonary aspergillosis
  • Aliases:
    • pulmonary aspergillus disease
Homo sapiens (human)
DOID:13258
  • typhoid fever
  • Aliases:
    • Typhoid
Homo sapiens (human)
DOID:0111768
  • X-linked properdin deficiency
  • Aliases:
    • CFPD
    • complement factor properdin deficiency
Homo sapiens (human)
DOID:0110934
  • nemaline myopathy 7
  • Aliases:
    • NEM7
    • nemaline myopathy 7, autosomal recessive
Homo sapiens (human)
DOID:11457
  • brain compression
Homo sapiens (human)
DOID:0050419
  • complement factor I deficiency
  • Aliases:
    • C3 INACTIVATOR DEFICIENCY
    • COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY
Homo sapiens (human)
DOID:0110025
  • age related macular degeneration 13
  • Aliases:
    • ARMD13
Homo sapiens (human)
DOID:0060746
  • basal laminar drusen
  • Aliases:
    • cuticular drusen
    • drusen of bruch membrane
    • early adult-onset grouped drusen
Homo sapiens (human)
DOID:2569
  • retinal drusen
Homo sapiens (human)
DOID:0110017
  • age related macular degeneration 4
  • Aliases:
    • ARMD4
Homo sapiens (human)
DOID:12030
  • panuveitis
  • Aliases:
    • Diffuse uveitis
Homo sapiens (human)
DOID:0060770
  • dextro-looped transposition of the great arteries
  • Aliases:
    • D-TGA
    • DTGA1
    • congenitally uncorrected transposition of the great arteries
    • congenitally uncorrected transposition of the great vessels
    • isolated ventriculoarterial discordance
    • ventriculoarterial discordance with atrioventricular concordance
Homo sapiens (human)
DOID:6406
  • double outlet right ventricle
  • Aliases:
    • Dextrotransposition of aorta
    • Double outlet right ventricle with subpulmonary ventricular septal defect
    • Taussig-Bing syndrome or defect
Homo sapiens (human)
DOID:12662
  • paracoccidioidomycosis
  • Aliases:
    • Mucocutaneous-lymphangitic paracoccidioidomycosis
    • paracoccidioidal mycosis
Homo sapiens (human)
DOID:0050127
  • sinusitis
Homo sapiens (human)
DOID:0111918
  • spermatogenic failure 40
  • Aliases:
    • SPGF40
Homo sapiens (human)
DOID:0112271
  • spermatogenic failure 49
  • Aliases:
    • SPGF98
Homo sapiens (human)

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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: December 9, 2024