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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 10876 - 10900 of 15957 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism Source
DOID:0081342
  • congenital myopathy 8
Mus musculus (house mouse)
DOID:0081342
  • congenital myopathy 8
Homo sapiens (human)
DOID:0081341
  • congenital myopathy 5
  • Aliases:
    • Salih myopathy
    • congenital myopathy-5 with cardiomyopathy
Homo sapiens (human)
DOID:0081341
  • congenital myopathy 5
  • Aliases:
    • Salih myopathy
    • congenital myopathy-5 with cardiomyopathy
Mus musculus (house mouse)
DOID:0081340
  • congenital myopathy 2C
Mus musculus (house mouse)
DOID:0081340
  • congenital myopathy 2C
Homo sapiens (human)
DOID:0081340
  • congenital myopathy 2C
Rattus norvegicus (Norway rat)
DOID:0081339
  • congenital myopathy 2B
Homo sapiens (human)
DOID:0081339
  • congenital myopathy 2B
Mus musculus (house mouse)
DOID:0081339
  • congenital myopathy 2B
Rattus norvegicus (Norway rat)
DOID:0081337
  • congenital myopathy
Homo sapiens (human)
DOID:0081337
  • congenital myopathy
Drosophila melanogaster (fruit fly)
DOID:0081337
  • congenital myopathy
Mus musculus (house mouse)
DOID:0081336
  • Thomsen disease
  • Aliases:
    • Congenital myotonia, autosomal dominant form
    • Thomsen's disease
Caenorhabditis elegans
DOID:0081335
  • Becker disease
Caenorhabditis elegans
DOID:0081333
  • Wiedemann-Rautenstrauch syndrome
  • Aliases:
    • Neonatal progeroid syndrome
    • PROGEROID SYNDROME, NEONATAL
Homo sapiens (human)
DOID:0081331
  • glycogen storage disease Ic
Homo sapiens (human)
DOID:0081330
  • glycogen storage disease Ib
Homo sapiens (human)
DOID:0081328
  • familial hyperinsulinemic hypoglycemia 8
Homo sapiens (human)
DOID:0081327
  • neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures
  • Aliases:
    • NEDAMSS
Mus musculus (house mouse)
DOID:0081327
  • neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures
  • Aliases:
    • NEDAMSS
Homo sapiens (human)
DOID:0081326
  • oxoglutarate dehydrogenase deficiency
  • Aliases:
    • Oxoglutaric aciduria
    • alpha-ketoglutarate dehydrogenase deficiency
Caenorhabditis elegans
DOID:0081326
  • oxoglutarate dehydrogenase deficiency
  • Aliases:
    • Oxoglutaric aciduria
    • alpha-ketoglutarate dehydrogenase deficiency
Homo sapiens (human)
DOID:0081326
  • oxoglutarate dehydrogenase deficiency
  • Aliases:
    • Oxoglutaric aciduria
    • alpha-ketoglutarate dehydrogenase deficiency
Rattus norvegicus (Norway rat)
DOID:0081326
  • oxoglutarate dehydrogenase deficiency
  • Aliases:
    • Oxoglutaric aciduria
    • alpha-ketoglutarate dehydrogenase deficiency
Xenopus laevis (African clawed frog)
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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