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 1026 - 1050 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism
DOID:1289
  • neurodegenerative disease
  • Aliases:
    • degenerative disease
Saccharomyces cerevisiae S288C
DOID:0080571
  • congenital disorder of glycosylation Iu
  • Aliases:
    • congenital disorder of glycosylation 1u
Homo sapiens (human)
DOID:9402
  • epididymitis
Homo sapiens (human)
DOID:0050674
  • congenital bile acid synthesis defect
  • Aliases:
    • 3-beta-hydroxy-delta-5-C27-steroid oxidoreductase deficiency
    • CBA
    • cholestasis with delta(4)-3-oxosteroid-5-beta-reductase deficiency
Homo sapiens (human)
DOID:9383
  • iridocyclitis
  • Aliases:
    • primary iridocyclitis
Homo sapiens (human)
DOID:0112198
  • spondyloepimetaphyseal dysplasia with joint laxity type 1
  • Aliases:
    • SEMDJL1
    • spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures
Caenorhabditis elegans
DOID:440
  • neuromuscular disease
Drosophila melanogaster (fruit fly)
DOID:0080759
  • Fanconi renotubular syndrome 3
Homo sapiens (human)
DOID:2474
  • vernal conjunctivitis
Homo sapiens (human)
DOID:0080162
  • lupus nephritis
Rattus norvegicus (Norway rat)
DOID:5075
  • myxopapillary ependymoma
Homo sapiens (human)
DOID:9281
  • phenylketonuria
  • Aliases:
    • Folling's disease
    • PKU
    • maternal phenylketonuria
    • phenylalaninemia
Homo sapiens (human)
DOID:0050833
  • orotic aciduria
Homo sapiens (human)
DOID:9370
  • obsolete exophthalmos
  • Aliases:
    • proptosis
Homo sapiens (human)
DOID:0112152
  • CHIME syndrome
  • Aliases:
    • PIGL-CDG
    • Zunich neuroectodermal syndrome
    • Zunich-Kaye syndrome
    • coloboma-congenital heart disease-ichthyosiform dermatosis-intellectual disability-ear anomalies syndrome
    • congenital disorder of glycosylation due to PIGL deficiency
    • neuroectodermal dysplasia, CHIME type
    • neuroectodermal syndrome, Zunich type
Homo sapiens (human)
DOID:3669
  • intermittent claudication
  • Aliases:
    • Charcot's syndrome
Homo sapiens (human)
DOID:0080559
  • congenital disorder of glycosylation Ig
  • Aliases:
    • ALG12-congenital disorder of glycosylation
    • congenital disorder of glycosylation 1g
Xenopus tropicalis (tropical clawed frog)
DOID:0111334
  • congenital leptin deficiency
  • Aliases:
    • LEPD
    • leptin deficiency or dysfunction
    • obesity due to congenital leptin deficiency
Homo sapiens (human)
DOID:0060892
  • late onset Parkinson's disease
  • Aliases:
    • late onset Parkinson disease
Mus musculus (house mouse)
DOID:0110341
  • osteogenesis imperfecta type 2
  • Aliases:
    • OI2
    • Vrolik type of osteogenesis imperfecta
    • osteogenesis imperfecta type II
    • perinatal lethal osteogenesis imperfecta congenita
Homo sapiens (human)
DOID:0050685
  • small cell carcinoma
  • Aliases:
    • Small cell carcinoma - intermediate cell
    • Small cell carcinoma, intermediate cell
    • intermediate cell small cell carcinoma
Saccharomyces cerevisiae S288C
DOID:552
  • pneumonia
  • Aliases:
    • acute pneumonia
Xenopus laevis (African clawed frog)
DOID:1791
  • peritoneal carcinoma
  • Aliases:
    • primary peritoneal carcinoma
Homo sapiens (human)
DOID:83
  • cataract
Caenorhabditis elegans
DOID:13580
  • cholestasis
  • Aliases:
    • Obstruction of bile duct
    • bile occlusion
Drosophila melanogaster (fruit fly)

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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