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 6026 - 6050 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:0081372
  • lacrimoauriculodentodigital syndrome 3
  • Aliases:
    • Lacrimo-auriculo-dento-digital syndrome 3
Mus musculus (house mouse)
DOID:2475
  • chronic conjunctivitis
Mus musculus (house mouse)
DOID:0050175
  • tick-borne encephalitis
  • Aliases:
    • Central European encephalitis
    • Far Eastern TBE
    • Russian spring-summer encephalitis
    • Siberian tick-borne encephalitis
    • Taiga encephalitis
    • Western European tick-borne encephalitis
    • west-Siberian encephalitis
Mus musculus (house mouse)
DOID:0080010
  • bone structure disease
Mus musculus (house mouse)
DOID:0110054
  • amelogenesis imperfecta type 1A
  • Aliases:
    • AI1A
    • amelogenesis imperfecta hypoplastic type IA
    • amelogenesis imperfecta type IA
Mus musculus (house mouse)
DOID:0110527
  • autosomal recessive nonsyndromic deafness 8
  • Aliases:
    • DFNB10
    • DFNB8
    • NRSD8
    • autosomal recessive deafness 10
    • autosomal recessive deafness 8
    • childhood-onset neurosensory autosomal recessive deafness 8
    • neurosensory nonsyndromic recessive deafness 8
Mus musculus (house mouse)
DOID:10632
  • Wolfram syndrome
  • Aliases:
    • WFS
Mus musculus (house mouse)
DOID:11563
  • retinal vasculitis
Mus musculus (house mouse)
DOID:0111130
  • focal segmental glomerulosclerosis 5
  • Aliases:
    • FSGS5
Mus musculus (house mouse)
DOID:0112282
  • spondyloepiphyseal dysplasia Kimberley type
  • Aliases:
    • SEDK
Mus musculus (house mouse)
DOID:4448
  • macular degeneration
  • Aliases:
    • Macular degeneration of retina
Mus musculus (house mouse)
DOID:0070443
  • neurodevelopmental disorder with cerebellar atrophy and motor dysfunction
Mus musculus (house mouse)
DOID:0110565
  • autosomal dominant nonsyndromic deafness 3B
  • Aliases:
    • DFNA3B
    • autosomal dominant deafness 3B
Mus musculus (house mouse)
DOID:2977
  • primary hyperoxaluria
Mus musculus (house mouse)
DOID:1724
  • duodenal ulcer
  • Aliases:
    • Curling Ulcer
    • Curling's ulcers
    • Stress Ulcer
Mus musculus (house mouse)
DOID:0070408
  • Hengel-Maroofian-Schols syndrome
Mus musculus (house mouse)
DOID:1574
  • alcohol use disorder
  • Aliases:
    • Ethanol abuse
    • alcohol abuse
Mus musculus (house mouse)
DOID:0060751
  • familial temporal lobe epilepsy 7
  • Aliases:
    • ETL7
Mus musculus (house mouse)
DOID:0110867
  • congenital stationary night blindness 1C
  • Aliases:
    • CSNB1C
    • congenital stationary night blindness 1C autosomal recessive
Mus musculus (house mouse)
DOID:0111991
  • immunodeficiency 62
  • Aliases:
    • IMD62
Mus musculus (house mouse)
DOID:0112370
  • Coffin-Siris syndrome 12
  • Aliases:
    • CSS12
Mus musculus (house mouse)
DOID:0080758
  • Fanconi renotubular syndrome 2
Mus musculus (house mouse)
DOID:0080592
  • Klippel-Feil syndrome 4
Mus musculus (house mouse)
DOID:11088
  • asphyxia neonatorum
  • Aliases:
    • Asphyxia - birth
    • Asphyxia, in liveborn infant
    • Birth asphyxia
    • postnatal asphyxia
Mus musculus (house mouse)
DOID:10140
  • dry eye syndrome
  • Aliases:
    • Tear film insufficiency
    • dry eye disease
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