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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 5051 - 5075 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:231
  • motor neuron disease
Drosophila melanogaster (fruit fly)
DOID:0060193
  • amyotrophic lateral sclerosis type 1
  • Aliases:
    • ALS1
    • amyotrophic lateral sclerosis 1
Drosophila melanogaster (fruit fly)
DOID:11713
  • diabetic angiopathy
  • Aliases:
    • Diabetic vascular disorder
    • diabetic peripheral angiopathy
Drosophila melanogaster (fruit fly)
DOID:10140
  • dry eye syndrome
  • Aliases:
    • Tear film insufficiency
    • dry eye disease
Drosophila melanogaster (fruit fly)
DOID:9111
  • cutaneous leishmaniasis
  • Aliases:
    • Asian Desert Cutaneous Leishmaniasis
    • Leproid leishmaniasis
    • diffuse cutaneous leishmaniasis
Drosophila melanogaster (fruit fly)
DOID:13544
  • low tension glaucoma
  • Aliases:
    • Normal tension glaucoma
Drosophila melanogaster (fruit fly)
DOID:0080322
  • polycystic kidney disease
Drosophila melanogaster (fruit fly)
DOID:2997
  • Sertoli-Leydig cell tumor
Homo sapiens (human)
DOID:0110345
  • osteogenesis imperfecta type 16
  • Aliases:
    • OI16
    • chromosome 11p11.2 deletion syndrome 91.3-KB
    • osteogenesis imperfecta type XVI
Rattus norvegicus (Norway rat)
DOID:0110658
  • congenital myasthenic syndrome 15
  • Aliases:
    • CMS15
    • congenital myasthenic syndrome 15 without tubular aggregates
Rattus norvegicus (Norway rat)
DOID:0111707
  • Bothnian type palmoplantar keratoderma
  • Aliases:
    • PPKB
    • diffuse palmoplantar keratoderma, Bothnian type
Homo sapiens (human)
DOID:0081202
  • autosomal recessive intellectual developmental disorder 37
Rattus norvegicus (Norway rat)
DOID:0110985
  • Joubert syndrome 16
  • Aliases:
    • JBTS16
Rattus norvegicus (Norway rat)
DOID:0050585
  • congenital generalized lipodystrophy
Rattus norvegicus (Norway rat)
DOID:0081401
  • autosomal dominant distal hereditary motor neuronopathy 13
Rattus norvegicus (Norway rat)
DOID:0110770
  • hereditary spastic paraplegia 17
  • Aliases:
    • SPG17
    • Silver spastic paraplegia syndrome
    • Silver syndrome
    • autosomal dominant spastic paraplegia 17
    • autosomal dominant spastic paraplegia type 17
    • dHMN5B
    • distal hereditary motor neuropathy type 5B
    • spastic paraplegia with amyotrophy of hands and feet
    • spastic paraplegia-amyotrophy of hands and feet
Rattus norvegicus (Norway rat)
DOID:0050661
  • vitelliform macular dystrophy
  • Aliases:
    • Best disease
    • Best macular dystrophy
    • juvenile-onset vitelliform macular dystrophy
Homo sapiens (human)
DOID:0060158
  • acquired metabolic disease
Rattus norvegicus (Norway rat)
DOID:0050729
  • Chanarin-Dorfman syndrome
  • Aliases:
    • neutral lipid storage disease
Rattus norvegicus (Norway rat)
DOID:0060354
  • Stormorken syndrome
  • Aliases:
    • thrombocytopathy, asplenia and miosis
Rattus norvegicus (Norway rat)
DOID:0080089
  • tubular aggregate myopathy 1
Rattus norvegicus (Norway rat)
DOID:0111970
  • immunodeficiency 10
  • Aliases:
    • CID due to STIM1 deficiency
    • IMD10
    • STIM1 deficiency
    • combined immunodeficiency due to STIM1 deficiency
    • immune dysfunction with T-cell inactivation due to calcium entry defect 2
Rattus norvegicus (Norway rat)
DOID:0080005
  • bone remodeling disease
Rattus norvegicus (Norway rat)
DOID:0111352
  • D-2-hydroxyglutaric aciduria 2
  • Aliases:
    • D2HGA2
Rattus norvegicus (Norway rat)
DOID:0110867
  • congenital stationary night blindness 1C
  • Aliases:
    • CSNB1C
    • congenital stationary night blindness 1C autosomal recessive
Rattus norvegicus (Norway rat)
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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