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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 4201 - 4225 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0070135
  • autosomal recessive cutis laxa type IA
  • Aliases:
    • ARCL1A
Rattus norvegicus (Norway rat)
DOID:0070290
  • primary autosomal recessive microcephaly 6
  • Aliases:
    • MCPH6
Drosophila melanogaster (fruit fly)
DOID:8499
  • night blindness
  • Aliases:
    • nyctalopia
Rattus norvegicus (Norway rat)
DOID:0080217
  • lysosomal acid lipase deficiency
  • Aliases:
    • LAL deficiency
    • LAL-D
Homo sapiens (human)
DOID:12971
  • hereditary spherocytosis
  • Aliases:
    • Congenital spherocytic hemolytic anemia
    • Minkowski Chauffard syndrome
    • spherocytic anemia
Rattus norvegicus (Norway rat)
DOID:0060308
  • autosomal recessive intellectual developmental disorder
  • Aliases:
    • autosomal recessive mental retardation
    • autosomal recessive non-syndromic mental retardation
Drosophila melanogaster (fruit fly)
DOID:1928
  • Williams-Beuren syndrome
  • Aliases:
    • Fanconi Schlesinger syndrome
    • WBS
Caenorhabditis elegans
DOID:9870
  • galactosemia
  • Aliases:
    • Galactosaemia
    • Galactose intolerance
Caenorhabditis elegans
DOID:1498
  • cholera
  • Aliases:
    • Cholera - Vibrio cholerae
    • Cholera due to Vibrio cholerae
    • Vibrio cholerae
Caenorhabditis elegans
DOID:0070038
  • autosomal dominant intellectual developmental disorder 8
  • Aliases:
    • MRD8
    • autosomal dominant mental retardation 8
    • autosomal dominant non-syndromic intellectual disability 8
Xenopus laevis (African clawed frog)
DOID:332
  • amyotrophic lateral sclerosis
  • Aliases:
    • ALS
    • Lou Gehrig's disease
    • motor neuron disease, bulbar
Danio rerio (zebrafish)
DOID:0060668
  • anencephaly
Danio rerio (zebrafish)
DOID:2566
  • corneal dystrophy
Mus musculus (house mouse)
DOID:0070462
  • mitochondrial complex V (ATP synthase) deficiency nuclear type 4B
  • Aliases:
    • MC5DN4B
Mus musculus (house mouse)
DOID:0090048
  • dystonia 16
Mus musculus (house mouse)
DOID:0070053
  • autosomal dominant intellectual developmental disorder 23
  • Aliases:
    • MRD23
    • autosomal dominant mental retardation 23
    • autosomal dominant non-syndromic intellectual disability 23
Homo sapiens (human)
DOID:0050645
  • arterial tortuosity syndrome
Homo sapiens (human)
DOID:916
  • liver benign neoplasm
  • Aliases:
    • epithelial hepatic and intrahepatic bile duct neoplasm
Saccharomyces cerevisiae S288C
DOID:0070045
  • Coffin-Siris syndrome 3
  • Aliases:
    • CSS3
    • MRD15
    • autosomal dominant mental retardation 15
Homo sapiens (human)
DOID:0050331
  • lacrimoauriculodentodigital syndrome 1
  • Aliases:
    • LEVY-HOLLISTER SYNDROME
    • Lacrimo-auriculo-dento-digital syndrome 1
Danio rerio (zebrafish)
DOID:0070233
  • Loeys-Dietz syndrome 4
  • Aliases:
    • Aneurysm, aortic and cerebral, with arterial tortuosity and skeletal manifestations
    • LDS4
Mus musculus (house mouse)
DOID:0080845
  • omodysplasia 2
Rattus norvegicus (Norway rat)
DOID:0110809
  • hereditary spastic paraplegia 57
  • Aliases:
    • SPG57
    • autosomal recessive spastic paraplegia 57
    • autosomal recessive spastic paraplegia type 57
Mus musculus (house mouse)
DOID:3204
  • schwannomatosis
  • Aliases:
    • SWN
    • neurilemmomatosis
    • neurinomatosis
Saccharomyces cerevisiae S288C
DOID:0050749
  • peripheral T-cell lymphoma
Homo sapiens (human)
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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