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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 8001 - 8025 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▲
DOID:0111847
  • osteogenesis imperfecta type 19
  • Aliases:
    • OI19
    • osteogenesis imperfecta type XIX
Mus musculus (house mouse)
DOID:0111849
  • osteogenesis imperfecta type 20
  • Aliases:
    • OI20
    • osteogenesis imperfecta type XX
Mus musculus (house mouse)
DOID:0111849
  • osteogenesis imperfecta type 20
  • Aliases:
    • OI20
    • osteogenesis imperfecta type XX
Rattus norvegicus (Norway rat)
DOID:0111849
  • osteogenesis imperfecta type 20
  • Aliases:
    • OI20
    • osteogenesis imperfecta type XX
Homo sapiens (human)
DOID:0111853
  • primary ciliary dyskinesia 40
  • Aliases:
    • CILD40
    • primary ciliary dyskinesia 40 with or without situs inversus
Homo sapiens (human)
DOID:0111854
  • primary ciliary dyskinesia 39
  • Aliases:
    • CILD39
    • primary ciliary dyskinesia 39 with or without situs inversus
Homo sapiens (human)
DOID:0111861
  • Meester-Loeys syndrome
  • Aliases:
    • MRLS
Rattus norvegicus (Norway rat)
DOID:0111861
  • Meester-Loeys syndrome
  • Aliases:
    • MRLS
Mus musculus (house mouse)
DOID:0111861
  • Meester-Loeys syndrome
  • Aliases:
    • MRLS
Homo sapiens (human)
DOID:0111862
  • congenital bilateral absence of vas deferens
  • Aliases:
    • CAVD
    • CBAVD
    • congenital bilateral agenesis of vas deferens
    • congenital bilateral aplasia of vas deferens
Mus musculus (house mouse)
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:0111862
  • congenital bilateral absence of vas deferens
  • Aliases:
    • CAVD
    • CBAVD
    • congenital bilateral agenesis of vas deferens
    • congenital bilateral aplasia of vas deferens
Saccharomyces cerevisiae S288C
DOID:0111862
  • congenital bilateral absence of vas deferens
  • Aliases:
    • CAVD
    • CBAVD
    • congenital bilateral agenesis of vas deferens
    • congenital bilateral aplasia of vas deferens
Danio rerio (zebrafish)
DOID:0111862
  • congenital bilateral absence of vas deferens
  • Aliases:
    • CAVD
    • CBAVD
    • congenital bilateral agenesis of vas deferens
    • congenital bilateral aplasia of vas deferens
Rattus norvegicus (Norway rat)
DOID:0111863
  • X-linked congenital bilateral absence of vas deferens
  • Aliases:
    • CBAVDX
Rattus norvegicus (Norway rat)
DOID:0111863
  • X-linked congenital bilateral absence of vas deferens
  • Aliases:
    • CBAVDX
Homo sapiens (human)
DOID:0111863
  • X-linked congenital bilateral absence of vas deferens
  • Aliases:
    • CBAVDX
Mus musculus (house mouse)
DOID:0111864
  • autosomal recessive congenital bilateral absence of vas deferens
Rattus norvegicus (Norway rat)
DOID:0111864
  • autosomal recessive congenital bilateral absence of vas deferens
Homo sapiens (human)
DOID:0111864
  • autosomal recessive congenital bilateral absence of vas deferens
Saccharomyces cerevisiae S288C
DOID:0111864
  • autosomal recessive congenital bilateral absence of vas deferens
Danio rerio (zebrafish)
DOID:0111864
  • autosomal recessive congenital bilateral absence of vas deferens
Mus musculus (house mouse)
DOID:0111865
  • MEND syndrome
  • Aliases:
    • male EBP disorder with neurological defects
Mus musculus (house mouse)
DOID:0111865
  • MEND syndrome
  • Aliases:
    • male EBP disorder with neurological defects
Homo sapiens (human)
DOID:0111866
  • trichothiodystrophy
  • Aliases:
    • TTD
Homo sapiens (human)
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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: December 9, 2024