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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 9501 - 9525 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲ Source
DOID:0070097
  • oculocutaneous albinism type III
  • Aliases:
    • OCA3
    • Rufous Oculocutaneous Albinism
Mus musculus (house mouse)
DOID:0080785
  • Brown-Vialetto-Van Laere syndrome 1
Mus musculus (house mouse)
DOID:1580
  • diffuse scleroderma
  • Aliases:
    • diffuse systemic sclerosis
    • systemic sclerosis, diffuse
Mus musculus (house mouse)
DOID:0080155
  • very long chain acyl-CoA dehydrogenase deficiency
  • Aliases:
    • VLCAD deficiency
Mus musculus (house mouse)
DOID:4603
  • epidermolytic hyperkeratosis
  • Aliases:
    • Bullous ichthyosiform erythroderma
    • Epidermolytic palmoplantar hyperkeratosis
    • epidermolytic ichthyosis
Mus musculus (house mouse)
DOID:12365
  • malaria
  • Aliases:
    • induced malaria
Mus musculus (house mouse)
DOID:1098
  • fetal erythroblastosis
  • Aliases:
    • EF - Erythroblastosis foetalis
    • Haemolytic disease due to rhesus isoimmunisation
    • erythroblastosis fetalis
    • rhesus isoimmunisation of the newborn
Mus musculus (house mouse)
DOID:0111377
  • fetal akinesia deformation sequence syndrome 1
  • Aliases:
    • FADS1
Mus musculus (house mouse)
DOID:0070098
  • oculocutaneous albinism type IV
  • Aliases:
    • OCA4
Mus musculus (house mouse)
DOID:0080528
  • bronchiectasis 3
Mus musculus (house mouse)
DOID:0111066
  • congenital bile acid synthesis defect 5
  • Aliases:
    • CBAS5
Mus musculus (house mouse)
DOID:0110276
  • autosomal recessive limb-girdle muscular dystrophy type 2B
  • Aliases:
    • LGMD2B
    • LGMD3
    • limb-girdle muscular dystrophy due to dysferlin deficiency
    • limb-girdle muscular dystrophy type 3
Mus musculus (house mouse)
DOID:0050912
  • colon adenoma
Mus musculus (house mouse)
DOID:0090001
  • Fraser syndrome
  • Aliases:
    • cryptophthalmos with other malformations
Mus musculus (house mouse)
DOID:0110218
  • Brugada syndrome 1
  • Aliases:
    • BRGDA1
Mus musculus (house mouse)
DOID:0070204
  • familial partial lipodystrophy type 3
  • Aliases:
    • FPLD3
    • PPARG-related FPLD
    • PPARG-related familial partial lipodystrophy
    • familial partial lipodystrophy associated with PPARG mutations
Mus musculus (house mouse)
DOID:4752
  • multiple system atrophy
  • Aliases:
    • Shy-Drager syndrome
Mus musculus (house mouse)
DOID:1094
  • attention deficit hyperactivity disorder
  • Aliases:
    • ADHD
    • attention deficit disorder
    • hyperkinetic disorder
Mus musculus (house mouse)
DOID:0111541
  • pigmented paravenous chorioretinal atrophy
  • Aliases:
    • PPRCA
Mus musculus (house mouse)
DOID:0111166
  • molybdenum cofactor deficiency type C
  • Aliases:
    • MOCOD type C
    • MOCODC
    • combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type C
    • molybdenum cofactor deficiency complementation group C
Mus musculus (house mouse)
DOID:0111134
  • focal segmental glomerulosclerosis 9
  • Aliases:
    • FSGS9
Mus musculus (house mouse)
DOID:11589
  • Riley-Day syndrome
  • Aliases:
    • HSAN III
    • familial autonomic nervous dysfunction
    • familial dysautonomia
Mus musculus (house mouse)
DOID:0111431
  • essential tremor 4
  • Aliases:
    • ETM4
    • hereditary essential tremor 4
Mus musculus (house mouse)
DOID:0080158
  • herpes simplex virus keratitis
  • Aliases:
    • dendritic keratitis
Mus musculus (house mouse)
DOID:0111542
  • familial expansile osteolysis
  • Aliases:
    • FEO
    • McCabe disease
    • hereditary expansile polyostotic osteolytic dysplasia
Mus musculus (house mouse)
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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