GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 2751 - 2775 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:0050648
  • atelosteogenesis
Homo sapiens (human)
DOID:0050841
  • focal hand dystonia
  • Aliases:
    • organic writer's cramp
Homo sapiens (human)
DOID:8867
  • molluscum contagiosum
Homo sapiens (human)
DOID:0060292
  • X-linked chondrodysplasia punctata 1
  • Aliases:
    • chondrodystrophia calcificans congenita
Homo sapiens (human)
DOID:0080110
  • contractures, pterygia, and spondylocarpotarsal fusion syndrome
  • Aliases:
    • multiple pterygium syndrome
Homo sapiens (human)
DOID:0110464
  • autosomal recessive nonsyndromic deafness 103
  • Aliases:
    • DFNB103
    • autosomal recessive deafness 103
Homo sapiens (human)
DOID:0050464
  • Farber lipogranulomatosis
  • Aliases:
    • Farber disease
    • N-laurylsphingosine deacylase deficiency
    • acid ceramidase deficiency
Homo sapiens (human)
DOID:0050336
  • hypophosphatemia
Homo sapiens (human)
DOID:3225
  • tracheal disease
Homo sapiens (human)
DOID:1591
  • renovascular hypertension
Homo sapiens (human)
DOID:0050471
  • Carney complex
  • Aliases:
    • Carney Complex, Type 1
    • Carney Complex, Type 2
    • Carney Syndrome
    • Carney complex variant
    • LAMB Syndrome
    • NAME Syndrome
Homo sapiens (human)
DOID:0070403
  • hypomyelinating leukodystrophy 26
  • Aliases:
    • HLD26
Homo sapiens (human)
DOID:0111103
  • maturity-onset diabetes of the young type 4
  • Aliases:
    • MODY type 4
    • MODY4
Homo sapiens (human)
DOID:4028
  • angioma serpiginosum
  • Aliases:
    • Angioma serpiginosum of skin
Homo sapiens (human)
DOID:0060074
  • ductal carcinoma in situ
Homo sapiens (human)
DOID:1678
  • chronic interstitial cystitis
Homo sapiens (human)
DOID:0110513
  • autosomal recessive nonsyndromic deafness 61
  • Aliases:
    • DFNB61
    • autosomal recessive deafness 61
Homo sapiens (human)
DOID:0060604
  • ankyloglossia
  • Aliases:
    • tongue-tie
Homo sapiens (human)
DOID:10327
  • anthracosis
  • Aliases:
    • Coal Miner's Pneumoconiosis
    • Coal workers' lung
    • Coal workers' pneumoconiosis
    • Melanoedema
    • black lung
Homo sapiens (human)
DOID:10141
  • obsolete asthenopia
Homo sapiens (human)
DOID:12803
  • Sly syndrome
  • Aliases:
    • MPS VII - Sly syndrome
    • beta-glucuronidase deficiency
    • deficiency of beta-glucuronidase
    • mucopolysaccharidosis VII
Homo sapiens (human)
DOID:0110453
  • dilated cardiomyopathy 1EE
  • Aliases:
    • CMD1EE
Homo sapiens (human)
DOID:0110764
  • hereditary spastic paraplegia 11
  • Aliases:
    • HSP-TCC
    • Nakamura-Osame syndrome
    • SPG11
    • autosomal recessive spastic paraplegia 11
    • autosomal recessive spastic paraplegia complicated with thin corpus callosum
    • autosomal recessive spastic paraplegia type 11
    • autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum
    • spastic paraplegia-intellectual disability-thin corpus callosum syndrome
Homo sapiens (human)
DOID:3951
  • acute myocarditis
Homo sapiens (human)
DOID:0080031
  • fibrous dysplasia
Homo sapiens (human)

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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: August 19, 2024