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 9751 - 9775 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:0080820
  • occupational asthma
Homo sapiens (human)
DOID:9849
  • Meniere's disease
  • Aliases:
    • Meniere disease
    • Mnire's vertigo
    • Otogenic vertigo
Homo sapiens (human)
DOID:3611
  • acute retinal necrosis syndrome
  • Aliases:
    • acute retinal necrosis
Homo sapiens (human)
DOID:0111079
  • birdshot chorioretinopathy
  • Aliases:
    • BSCR
    • birdshot chorioretinitis
    • birdshot retinochoroiditis
    • birdshot retinochoroidopathy
    • vitiliginous choroiditis
Homo sapiens (human)
DOID:11265
  • trachoma
  • Aliases:
    • active stage trachoma
    • trachoma dubium
Homo sapiens (human)
DOID:0080750
  • erythema nodosum
Homo sapiens (human)
DOID:3875
  • thrombophlebitis
  • Aliases:
    • Phlebitis and thrombophlebitis of superficial vessels of lower extremities
    • Superficial thrombophlebitis of leg
    • Thrombophlebitis of a superficial leg vein
    • Thrombophlebitis of superficial veins of lower extremity
Homo sapiens (human)
DOID:2703
  • synovitis
Homo sapiens (human)
DOID:0080160
  • Cytomegalovirus retinitis
  • Aliases:
    • CMV retinitis
Homo sapiens (human)
DOID:11563
  • retinal vasculitis
Homo sapiens (human)
DOID:0070048
  • GAND syndrome
  • Aliases:
    • MRD18
    • autosomal dominant intellectual developmental disorder 18
    • autosomal dominant mental retardation 18
    • autosomal dominant non-syndromic intellectual disability 18
Rattus norvegicus (Norway rat)
DOID:0070067
  • White-Sutton syndrome
  • Aliases:
    • MRD37
    • WHSUS
    • autosomal dominant mental retardation 37
Rattus norvegicus (Norway rat)
DOID:0111648
  • ectopia lentis with ectopia of pupil
  • Aliases:
    • ectopia lentis et pupillae
Rattus norvegicus (Norway rat)
DOID:0111149
  • autosomal recessive isolated ectopia lentis 2
  • Aliases:
    • ECTOL2
Rattus norvegicus (Norway rat)
DOID:110
  • lens disease
Rattus norvegicus (Norway rat)
DOID:0112266
  • nephrotic syndrome type 23
  • Aliases:
    • NPHS23
Rattus norvegicus (Norway rat)
DOID:0111286
  • psoriasis 1
  • Aliases:
    • PSORS1
Homo sapiens (human)
DOID:431
  • myofascial pain syndrome
Rattus norvegicus (Norway rat)
DOID:0080809
  • chronic asthma
Rattus norvegicus (Norway rat)
DOID:12143
  • neurogenic bladder
  • Aliases:
    • Neuropathic bladder
    • neurogenic dysfunction of the urinary bladder
    • neurogenic urinary bladder disorder
Rattus norvegicus (Norway rat)
DOID:10685
  • separation anxiety disorder
Rattus norvegicus (Norway rat)
DOID:0070145
  • hereditary sensory and autonomic neuropathy type 5
  • Aliases:
    • HSAN5
    • hereditary sensory and autonomic neuropathy type V
Rattus norvegicus (Norway rat)
DOID:3633
  • beta-mannosidosis
  • Aliases:
    • Beta-D-mannosidosis
    • beta-mannosidase deficiency
    • lysosomal beta-mannosidase deficiency
Rattus norvegicus (Norway rat)
DOID:14250
  • Down syndrome
  • Aliases:
    • Complete trisomy 21 syndrome
    • Down's syndrome
    • Down's syndrome - trisomy 21
    • Downs syndrome
    • G Trisomy
    • trisomy 21 syndrome
Drosophila melanogaster (fruit fly)
DOID:0111546
  • Currarino syndrome
  • Aliases:
    • Currarino triad
Homo sapiens (human)

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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