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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 12676 - 12700 of 15957 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism Source
DOID:0080042
  • autosomal recessive spinocerebellar ataxia 18
  • Aliases:
    • SCAR18
Danio rerio (zebrafish)
DOID:0080041
  • hypochondroplasia
Xenopus laevis (African clawed frog)
DOID:0080041
  • hypochondroplasia
Drosophila melanogaster (fruit fly)
DOID:0080041
  • hypochondroplasia
Homo sapiens (human)
DOID:0080038
  • pycnodysostosis
Rattus norvegicus (Norway rat)
DOID:0080038
  • pycnodysostosis
Mus musculus (house mouse)
DOID:0080038
  • pycnodysostosis
Homo sapiens (human)
DOID:0080037
  • Worth syndrome
  • Aliases:
    • Worth's syndrome
    • autosomal dominant endosteal hyperostosis
    • autosomal dominant osteosclerosis
    • benign form of Worth hyperostosis corticalis generalisata with torus platinus
Homo sapiens (human)
DOID:0080037
  • Worth syndrome
  • Aliases:
    • Worth's syndrome
    • autosomal dominant endosteal hyperostosis
    • autosomal dominant osteosclerosis
    • benign form of Worth hyperostosis corticalis generalisata with torus platinus
Mus musculus (house mouse)
DOID:0080036
  • SOST-related sclerosing bone dysplasia
  • Aliases:
    • van Buchem disease
Homo sapiens (human)
DOID:0080036
  • SOST-related sclerosing bone dysplasia
  • Aliases:
    • van Buchem disease
Mus musculus (house mouse)
DOID:0080036
  • SOST-related sclerosing bone dysplasia
  • Aliases:
    • van Buchem disease
Rattus norvegicus (Norway rat)
DOID:0080030
  • spondyloepimetaphyseal dysplasia, Missouri type
Caenorhabditis elegans
DOID:0080030
  • spondyloepimetaphyseal dysplasia, Missouri type
Mus musculus (house mouse)
DOID:0080030
  • spondyloepimetaphyseal dysplasia, Missouri type
Homo sapiens (human)
DOID:0080028
  • spondyloepimetaphyseal dysplasia, Strudwick type
Mus musculus (house mouse)
DOID:0080028
  • spondyloepimetaphyseal dysplasia, Strudwick type
Rattus norvegicus (Norway rat)
DOID:0080028
  • spondyloepimetaphyseal dysplasia, Strudwick type
Homo sapiens (human)
DOID:0080028
  • spondyloepimetaphyseal dysplasia, Strudwick type
Xenopus tropicalis (tropical clawed frog)
DOID:0080028
  • spondyloepimetaphyseal dysplasia, Strudwick type
Xenopus laevis (African clawed frog)
DOID:0080027
  • spondyloepimetaphyseal dysplasia
Xenopus tropicalis (tropical clawed frog)
DOID:0080027
  • spondyloepimetaphyseal dysplasia
Rattus norvegicus (Norway rat)
DOID:0080027
  • spondyloepimetaphyseal dysplasia
Homo sapiens (human)
DOID:0080027
  • spondyloepimetaphyseal dysplasia
Mus musculus (house mouse)
DOID:0080026
  • otospondylomegaepiphyseal dysplasia, autosomal recessive
  • Aliases:
    • CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS
    • NANCE-INSLEY SYNDROME
    • NANCE-SWEENEY CHONDRODYSPLASIA
    • OSMEDB
Mus musculus (house mouse)
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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