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 1276 - 1300 of 7942 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism
DOID:0070460
  • hereditary spastic paraplegia 90B
  • Aliases:
    • SPG90B
    • autosomal recessive spastic paraplegia 90B
Homo sapiens (human)
DOID:0070467
  • carpal tunnel syndrome 2
  • Aliases:
    • CTS2
Drosophila melanogaster (fruit fly)
DOID:0070468
  • Yoon-Bellen neurodevelopmental syndrome
  • Aliases:
    • YOBELN
Xenopus laevis (African clawed frog)
DOID:0070468
  • Yoon-Bellen neurodevelopmental syndrome
  • Aliases:
    • YOBELN
Homo sapiens (human)
DOID:0070468
  • Yoon-Bellen neurodevelopmental syndrome
  • Aliases:
    • YOBELN
Caenorhabditis elegans
DOID:0070468
  • Yoon-Bellen neurodevelopmental syndrome
  • Aliases:
    • YOBELN
Rattus norvegicus (Norway rat)
DOID:0070468
  • Yoon-Bellen neurodevelopmental syndrome
  • Aliases:
    • YOBELN
Mus musculus (house mouse)
DOID:0070516
  • Mitchell syndrome
Drosophila melanogaster (fruit fly)
DOID:0070516
  • Mitchell syndrome
Homo sapiens (human)
DOID:0070519
  • early-onset vitamin B6-dependent epilepsy 4
  • Aliases:
    • AASA dehydrogenase deficiency
    • EPEO4
    • PDE-ALDH7A1
    • antiquitin deficiency
Homo sapiens (human)
DOID:0080000
  • muscular disease
Drosophila melanogaster (fruit fly)
DOID:0080000
  • muscular disease
Homo sapiens (human)
DOID:0080001
  • bone disease
Homo sapiens (human)
DOID:0080005
  • bone remodeling disease
Saccharomyces cerevisiae S288C
DOID:0080005
  • bone remodeling disease
Mus musculus (house mouse)
DOID:0080005
  • bone remodeling disease
Homo sapiens (human)
DOID:0080005
  • bone remodeling disease
Rattus norvegicus (Norway rat)
DOID:0080011
  • bone resorption disease
Homo sapiens (human)
DOID:0080016
  • spina bifida
Homo sapiens (human)
DOID:0080021
  • Schmid metaphyseal chondrodysplasia
  • Aliases:
    • Japanese type spondylometaphyseal dysplasia
    • Schmid type metaphyseal dysplasia
Homo sapiens (human)
DOID:0080028
  • spondyloepimetaphyseal dysplasia, Strudwick type
Homo sapiens (human)
DOID:0080029
  • autosomal recessive spinocerebellar ataxia 16
  • Aliases:
    • SCAR16
Homo sapiens (human)
DOID:0080031
  • fibrous dysplasia
Homo sapiens (human)
DOID:0080033
  • craniometaphyseal dysplasia
Homo sapiens (human)
DOID:0080036
  • SOST-related sclerosing bone dysplasia
  • Aliases:
    • van Buchem disease
Homo sapiens (human)

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: August 19, 2024