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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 12701 - 12725 of 15957 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism Source
DOID:0080026
  • otospondylomegaepiphyseal dysplasia, autosomal recessive
  • Aliases:
    • CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS
    • NANCE-INSLEY SYNDROME
    • NANCE-SWEENEY CHONDRODYSPLASIA
    • OSMEDB
Homo sapiens (human)
DOID:0080021
  • Schmid metaphyseal chondrodysplasia
  • Aliases:
    • Japanese type spondylometaphyseal dysplasia
    • Schmid type metaphyseal dysplasia
Homo sapiens (human)
DOID:0080020
  • Jansen's metaphyseal chondrodysplasia
  • Aliases:
    • Jansen Disease
    • Jansen Metaphyseal Dysostosis
    • Jansen metaphyseal chondrodysplasia
    • Murk Jansen Type Metaphyseal Chondrodysplasia
Rattus norvegicus (Norway rat)
DOID:0080020
  • Jansen's metaphyseal chondrodysplasia
  • Aliases:
    • Jansen Disease
    • Jansen Metaphyseal Dysostosis
    • Jansen metaphyseal chondrodysplasia
    • Murk Jansen Type Metaphyseal Chondrodysplasia
Mus musculus (house mouse)
DOID:0080020
  • Jansen's metaphyseal chondrodysplasia
  • Aliases:
    • Jansen Disease
    • Jansen Metaphyseal Dysostosis
    • Jansen metaphyseal chondrodysplasia
    • Murk Jansen Type Metaphyseal Chondrodysplasia
Caenorhabditis elegans
DOID:0080020
  • Jansen's metaphyseal chondrodysplasia
  • Aliases:
    • Jansen Disease
    • Jansen Metaphyseal Dysostosis
    • Jansen metaphyseal chondrodysplasia
    • Murk Jansen Type Metaphyseal Chondrodysplasia
Homo sapiens (human)
DOID:0080019
  • metaphyseal dysplasia
  • Aliases:
    • Bakwin-Krida syndrome
    • Pyle's disease
    • Pyle-Cohn syndrome
Mus musculus (house mouse)
DOID:0080019
  • metaphyseal dysplasia
  • Aliases:
    • Bakwin-Krida syndrome
    • Pyle's disease
    • Pyle-Cohn syndrome
Homo sapiens (human)
DOID:0080019
  • metaphyseal dysplasia
  • Aliases:
    • Bakwin-Krida syndrome
    • Pyle's disease
    • Pyle-Cohn syndrome
Rattus norvegicus (Norway rat)
DOID:0080016
  • spina bifida
Drosophila melanogaster (fruit fly)
DOID:0080016
  • spina bifida
Mus musculus (house mouse)
DOID:0080016
  • spina bifida
Caenorhabditis elegans
DOID:0080016
  • spina bifida
Homo sapiens (human)
DOID:0080015
  • physical disorder
  • Aliases:
    • congenital disorder
Homo sapiens (human)
DOID:0080015
  • physical disorder
  • Aliases:
    • congenital disorder
Caenorhabditis elegans
DOID:0080015
  • physical disorder
  • Aliases:
    • congenital disorder
Mus musculus (house mouse)
DOID:0080015
  • physical disorder
  • Aliases:
    • congenital disorder
Drosophila melanogaster (fruit fly)
DOID:0080010
  • bone structure disease
Mus musculus (house mouse)
DOID:0080010
  • bone structure disease
Saccharomyces cerevisiae S288C
DOID:0080010
  • bone structure disease
Rattus norvegicus (Norway rat)
DOID:0080010
  • bone structure disease
Homo sapiens (human)
DOID:0080006
  • bone development disease
Rattus norvegicus (Norway rat)
DOID:0080006
  • bone development disease
Mus musculus (house mouse)
DOID:0080006
  • bone development disease
Homo sapiens (human)
DOID:0080006
  • bone development disease
Danio rerio (zebrafish)
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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