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 10376 - 10400 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲ Source
DOID:631
  • fibromyalgia
Mus musculus (house mouse)
DOID:0060799
  • syndromic X-linked intellectual disability Lubs type
  • Aliases:
    • Lubs X-linked mental retardation syndrome
    • MECP2 duplication syndrome
    • MRXSL
    • X-linked intellectual disability-hypotonia-recurrent Infections syndrome
    • mental retardation, X-linked, syndromic, Lubs type
    • mental retardation, X-linked, with recurrent respiratory infections
Mus musculus (house mouse)
DOID:0080242
  • syndromic X-linked mental retardation Hough type
Mus musculus (house mouse)
DOID:0110475
  • autosomal recessive nonsyndromic deafness 1A
  • Aliases:
    • DFNB1A
    • autosomal recessive deafness 1A
Mus musculus (house mouse)
DOID:0112199
  • spondyloepimetaphyseal dysplasia with joint laxity type 2
  • Aliases:
    • SEMD-MD
    • SEMDJL2
    • spondyloepimetaphyseal dysplasia with joint laxicity, Hall type
    • spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type
    • spondyloepimetaphyseal dysplasia with multiple dislocations, Hall type
Mus musculus (house mouse)
DOID:0070118
  • Meckel syndrome 4
  • Aliases:
    • MKS4
    • Meckel-Gruber syndrome, type 4
Mus musculus (house mouse)
DOID:0081324
  • neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss
  • Aliases:
    • NEDGTH
Mus musculus (house mouse)
DOID:0110014
  • age related macular degeneration 1
  • Aliases:
    • ARMD1
    • age related maculopathy 1
Mus musculus (house mouse)
DOID:10316
  • pneumoconiosis
Mus musculus (house mouse)
DOID:0110021
  • age related macular degeneration 9
  • Aliases:
    • ARMD9
Mus musculus (house mouse)
DOID:0050433
  • fatal familial insomnia
Mus musculus (house mouse)
DOID:0080095
  • myofibrillar myopathy 4
  • Aliases:
    • zaspopathy
Mus musculus (house mouse)
DOID:350
  • mastocytosis
  • Aliases:
    • mast cell hyperplasia
Mus musculus (house mouse)
DOID:0050605
  • acrodermatitis enteropathica
Mus musculus (house mouse)
DOID:0080377
  • peroxisomal biogenesis disorder
Mus musculus (house mouse)
DOID:0110446
  • dilated cardiomyopathy 1W
  • Aliases:
    • CMD1W
Mus musculus (house mouse)
DOID:0060835
  • isolated microphthalmia 6
  • Aliases:
    • MCOP6
    • posterior nonsyndromic microphthalmia
Mus musculus (house mouse)
DOID:0050905
  • inflammatory myofibroblastic tumor
Mus musculus (house mouse)
DOID:0090111
  • PCWH syndrome
  • Aliases:
    • Neurologic Waardenburg-Shah syndrome
    • PCWH
    • Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease
    • Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Hirschsprung disease-Waardenburg syndrome
Mus musculus (house mouse)
DOID:11664
  • nephrosclerosis
  • Aliases:
    • renal sclerosis
Mus musculus (house mouse)
DOID:0111007
  • X-linked cone-rod dystrophy 3
  • Aliases:
    • CORDX3
Mus musculus (house mouse)
DOID:4481
  • allergic rhinitis
  • Aliases:
    • Non-seasonal allergic rhinitis
    • Perenial allergic rhinitis
    • atopic rhinitis
    • hay fever
    • pollenosis
    • seasonal allergic rhinitis
Mus musculus (house mouse)
DOID:4906
  • small intestine adenocarcinoma
  • Aliases:
    • small intestinal adenocarcinoma
Mus musculus (house mouse)
DOID:0110858
  • polycystic kidney disease 1
  • Aliases:
    • Apkd1
    • Pkd1
    • Polycystic Kidney Disease, Adult, Type I
Mus musculus (house mouse)
DOID:0111391
  • mucopolysaccharidosis IVA
  • Aliases:
    • GALNS deficiency
    • MPS IVA
    • MPS4A
    • Morquio A disease
    • Morquio syndrome A
Mus musculus (house mouse)

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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