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 11826 - 11850 of 15957 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism Source
DOID:633
  • myositis
  • Aliases:
    • Inflammatory disorder of muscle
Rattus norvegicus (Norway rat)
DOID:633
  • myositis
  • Aliases:
    • Inflammatory disorder of muscle
Homo sapiens (human)
DOID:633
  • myositis
  • Aliases:
    • Inflammatory disorder of muscle
Mus musculus (house mouse)
DOID:0111072
  • myostatin-related muscle hypertrophy
  • Aliases:
    • MSLHP
Homo sapiens (human)
DOID:0111072
  • myostatin-related muscle hypertrophy
  • Aliases:
    • MSLHP
Danio rerio (zebrafish)
DOID:0111072
  • myostatin-related muscle hypertrophy
  • Aliases:
    • MSLHP
Caenorhabditis elegans
DOID:0111072
  • myostatin-related muscle hypertrophy
  • Aliases:
    • MSLHP
Mus musculus (house mouse)
DOID:0111072
  • myostatin-related muscle hypertrophy
  • Aliases:
    • MSLHP
Rattus norvegicus (Norway rat)
DOID:2106
  • myotonia congenita
  • Aliases:
    • Batten Turner congenital myopathy
    • Thomsen and Becker disease
Caenorhabditis elegans
DOID:2106
  • myotonia congenita
  • Aliases:
    • Batten Turner congenital myopathy
    • Thomsen and Becker disease
Mus musculus (house mouse)
DOID:2106
  • myotonia congenita
  • Aliases:
    • Batten Turner congenital myopathy
    • Thomsen and Becker disease
Homo sapiens (human)
DOID:450
  • myotonic disease
Homo sapiens (human)
DOID:11722
  • myotonic dystrophy type 1
  • Aliases:
    • Dystrophia myotonica
    • Steinert disease
    • congenital myotonic dystrophy
    • myotonic dystrophy of Steinert
Mus musculus (house mouse)
DOID:11722
  • myotonic dystrophy type 1
  • Aliases:
    • Dystrophia myotonica
    • Steinert disease
    • congenital myotonic dystrophy
    • myotonic dystrophy of Steinert
Drosophila melanogaster (fruit fly)
DOID:11722
  • myotonic dystrophy type 1
  • Aliases:
    • Dystrophia myotonica
    • Steinert disease
    • congenital myotonic dystrophy
    • myotonic dystrophy of Steinert
Homo sapiens (human)
DOID:0050759
  • myotonic dystrophy type 2
Homo sapiens (human)
DOID:9467
  • nail-patella syndrome
  • Aliases:
    • Fong disease
    • Turner-Kiser syndrome
    • hereditary onychoostedysplasia
    • iliac horn syndrome
    • nail patella syndrome
Homo sapiens (human)
DOID:9467
  • nail-patella syndrome
  • Aliases:
    • Fong disease
    • Turner-Kiser syndrome
    • hereditary onychoostedysplasia
    • iliac horn syndrome
    • nail patella syndrome
Mus musculus (house mouse)
DOID:0080634
  • nanophthalmos
Xenopus laevis (African clawed frog)
DOID:0080634
  • nanophthalmos
Homo sapiens (human)
DOID:0080634
  • nanophthalmos
Mus musculus (house mouse)
DOID:0080634
  • nanophthalmos
Caenorhabditis elegans
DOID:8986
  • narcolepsy
  • Aliases:
    • Narcolepsy, without cataplexy
    • paroxysmal sleep
Rattus norvegicus (Norway rat)
DOID:8986
  • narcolepsy
  • Aliases:
    • Narcolepsy, without cataplexy
    • paroxysmal sleep
Mus musculus (house mouse)
DOID:8986
  • narcolepsy
  • Aliases:
    • Narcolepsy, without cataplexy
    • paroxysmal sleep
Homo sapiens (human)

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 9, 2024