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 14551 - 14575 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:0070536
  • neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures
  • Aliases:
    • NEDHLSS
Danio rerio (zebrafish)
DOID:12143
  • neurogenic bladder
  • Aliases:
    • Neuropathic bladder
    • neurogenic dysfunction of the urinary bladder
    • neurogenic urinary bladder disorder
Danio rerio (zebrafish)
DOID:0080006
  • bone development disease
Danio rerio (zebrafish)
DOID:0060695
  • hyperekplexia
  • Aliases:
    • Kok disease
    • congenital stiff man syndrome
    • familial startle disease
    • hereditary hyperekplexia
    • startle disease
Danio rerio (zebrafish)
DOID:9828
  • neonatal abstinence syndrome
  • Aliases:
    • Drug withdrawal syndrome in newborn
Danio rerio (zebrafish)
DOID:10754
  • otitis media
Danio rerio (zebrafish)
DOID:0111864
  • autosomal recessive congenital bilateral absence of vas deferens
Danio rerio (zebrafish)
DOID:14067
  • Plasmodium falciparum malaria
  • Aliases:
    • Malaria fever, subtertian
    • falciparum malaria
    • malignant tertian fever
Danio rerio (zebrafish)
DOID:0110633
  • rigid spine muscular dystrophy 1
  • Aliases:
    • Eichsfeld type congenital muscular dystrophy
    • MDRS1
    • RSMD1
    • RSS
    • SEPN1-related myopathy
    • classic MmD
    • classic multiminicore disease
    • classic multiminicore myopathy
    • congenital merosin-positive muscular dystrophy with early spine rigidity
    • desmin-related myopathy with Mallory bodies
    • desmin-related myopathy with Mallory body-like inclusions
    • early-onset desmin-related myopathy
    • rigid spine syndrome
    • severe classic form minicore myopathy
    • severe classic form multicore myopathy
    • severe classic form multiminicore disease
Danio rerio (zebrafish)
DOID:0080809
  • chronic asthma
Danio rerio (zebrafish)
DOID:9993
  • hypoglycemia
  • Aliases:
    • Hypoglycaemia
Danio rerio (zebrafish)
DOID:0110299
  • autosomal recessive limb-girdle muscular dystrophy type 2I
  • Aliases:
    • LGMD2I
    • Limb-girdle muscular dystrophy due to FKRP deficiency
    • MDDGC5
    • muscular dystrophy limb-girdle type 2I
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C 5
    • muscular dystrophy-dystroglycanopathy limb-girdle FRKP-related
Danio rerio (zebrafish)
DOID:9976
  • heroin dependence
Danio rerio (zebrafish)
DOID:0110975
  • brachydactyly type B2
  • Aliases:
    • BDB2
Danio rerio (zebrafish)
DOID:13207
  • proliferative diabetic retinopathy
  • Aliases:
    • PDR
Danio rerio (zebrafish)
DOID:0110372
  • retinitis pigmentosa 4
  • Aliases:
    • RP4
Danio rerio (zebrafish)
DOID:0111337
  • Jackson-Weiss syndrome
  • Aliases:
    • JWS
    • craniosynostosis-midfacial hypoplasia-foot abnormalities syndrome
Danio rerio (zebrafish)
DOID:4247
  • coronary restenosis
Danio rerio (zebrafish)
DOID:10126
  • keratoconus
  • Aliases:
    • conical cornea
Danio rerio (zebrafish)
DOID:13406
  • pulmonary sarcoidosis
  • Aliases:
    • lung Sarcoidosis
Danio rerio (zebrafish)
DOID:1094
  • attention deficit hyperactivity disorder
  • Aliases:
    • ADHD
    • attention deficit disorder
    • hyperkinetic disorder
Danio rerio (zebrafish)
DOID:9408
  • acute myocardial infarction
Danio rerio (zebrafish)
DOID:10211
  • cholelithiasis
Danio rerio (zebrafish)
DOID:0080526
  • bronchiectasis 1
Danio rerio (zebrafish)
DOID:0070309
  • absence epilepsy
Danio rerio (zebrafish)

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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