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 4701 - 4725 of 7942 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism
DOID:0112361
  • spondylocostal dysostosis 3
  • Aliases:
    • SCDO3
    • autosomal recessive spondylocostal dysostosis 3
Drosophila melanogaster (fruit fly)
DOID:0112361
  • spondylocostal dysostosis 3
  • Aliases:
    • SCDO3
    • autosomal recessive spondylocostal dysostosis 3
Mus musculus (house mouse)
DOID:0112361
  • spondylocostal dysostosis 3
  • Aliases:
    • SCDO3
    • autosomal recessive spondylocostal dysostosis 3
Danio rerio (zebrafish)
DOID:0112361
  • spondylocostal dysostosis 3
  • Aliases:
    • SCDO3
    • autosomal recessive spondylocostal dysostosis 3
Xenopus laevis (African clawed frog)
DOID:0112361
  • spondylocostal dysostosis 3
  • Aliases:
    • SCDO3
    • autosomal recessive spondylocostal dysostosis 3
Xenopus tropicalis (tropical clawed frog)
DOID:0112361
  • spondylocostal dysostosis 3
  • Aliases:
    • SCDO3
    • autosomal recessive spondylocostal dysostosis 3
Rattus norvegicus (Norway rat)
DOID:0112361
  • spondylocostal dysostosis 3
  • Aliases:
    • SCDO3
    • autosomal recessive spondylocostal dysostosis 3
Homo sapiens (human)
DOID:0112349
  • hereditary spastic paraplegia 81
  • Aliases:
    • SPG81
    • autosomal recessive complex SPG due to Kennedy pathway dysfunction
    • autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction
    • spastic paraplegia 81 autosomal recessive
Homo sapiens (human)
DOID:0112347
  • hereditary spastic paraplegia 84
  • Aliases:
    • SPG84
    • spastic paraplegia 84 autosomal recessive
Homo sapiens (human)
DOID:0112343
  • hereditary spastic paraplegia 82
  • Aliases:
    • SPG82
    • spastic paraplegia 82 autosomal recessive
Homo sapiens (human)
DOID:0112333
  • pontocerebellar hypoplasia type 16
  • Aliases:
    • PCH16
Homo sapiens (human)
DOID:0112321
  • alacrima, achalasia, and impaired intellectual development syndrome
  • Aliases:
    • AAMR
    • alacrima, achalasia, and mental retardation syndrome
Homo sapiens (human)
DOID:0112319
  • Kanzaki disease
  • Aliases:
    • NAGA deficiency type 2
    • adult-onset alpha-N-acetylgalactosaminidase deficiency
    • alpha-N-acetylgalactosaminidase deficiency type 2
Mus musculus (house mouse)
DOID:0112319
  • Kanzaki disease
  • Aliases:
    • NAGA deficiency type 2
    • adult-onset alpha-N-acetylgalactosaminidase deficiency
    • alpha-N-acetylgalactosaminidase deficiency type 2
Homo sapiens (human)
DOID:0112319
  • Kanzaki disease
  • Aliases:
    • NAGA deficiency type 2
    • adult-onset alpha-N-acetylgalactosaminidase deficiency
    • alpha-N-acetylgalactosaminidase deficiency type 2
Rattus norvegicus (Norway rat)
DOID:0112318
  • Schindler disease type 1
  • Aliases:
    • NAGA deficiency type 1
    • alpha-N-acetylgalactosaminidase deficiency type 1
Homo sapiens (human)
DOID:0112318
  • Schindler disease type 1
  • Aliases:
    • NAGA deficiency type 1
    • alpha-N-acetylgalactosaminidase deficiency type 1
Mus musculus (house mouse)
DOID:0112318
  • Schindler disease type 1
  • Aliases:
    • NAGA deficiency type 1
    • alpha-N-acetylgalactosaminidase deficiency type 1
Rattus norvegicus (Norway rat)
DOID:0112315
  • brain small vessel disease 3
  • Aliases:
    • BSVD3
Drosophila melanogaster (fruit fly)
DOID:0112315
  • brain small vessel disease 3
  • Aliases:
    • BSVD3
Mus musculus (house mouse)
DOID:0112315
  • brain small vessel disease 3
  • Aliases:
    • BSVD3
Rattus norvegicus (Norway rat)
DOID:0112315
  • brain small vessel disease 3
  • Aliases:
    • BSVD3
Danio rerio (zebrafish)
DOID:0112315
  • brain small vessel disease 3
  • Aliases:
    • BSVD3
Caenorhabditis elegans
DOID:0112315
  • brain small vessel disease 3
  • Aliases:
    • BSVD3
Homo sapiens (human)
DOID:0112315
  • brain small vessel disease 3
  • Aliases:
    • BSVD3
Xenopus laevis (African clawed frog)

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Last updated: August 19, 2024