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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 9351 - 9375 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:5325
  • Roberts syndrome
  • Aliases:
    • LONG BONE DEFICIENCIES ASSOCIATED WITH CLEFT LIP-PALATE
    • RBS
    • Roberts-Sc Phocomelia Syndrome
    • SC phocomelia syndrome
Mus musculus (house mouse)
DOID:0111401
  • congenital dyserythropoietic anemia type II
  • Aliases:
    • CDA II
    • CDA type 2
    • CDA type II
    • CDAN2
    • Congenital dyserythropoietic anaemia type 2
    • Congenital dyserythropoietic anemia type 2
    • Hereditary erythroblastic multinuclearity with a positive acidified-serum test (hempas)
    • SEC23B-CDG
    • congenital dyserythropoietic anaemia type II
Mus musculus (house mouse)
DOID:0060319
  • cardiac arrest
  • Aliases:
    • cardiopulmonary arrest
    • circulatory arrest
Homo sapiens (human)
DOID:0060213
  • frontotemporal dementia and/or amyotrophic lateral sclerosis 1
  • Aliases:
    • ALSFTD
    • FTDALS1
    • FTDMND
    • amyotrophic lateral sclerosis and/or frontotemporal dementia
    • frontotemporal dementia and/or motor neuron disease
Homo sapiens (human)
DOID:0081427
  • autosomal recessive distal hereditary motor neuronopathy 8
  • Aliases:
    • SORDD
    • sorbitol dehydrogenase deficiency with peripheral neuropathy
Mus musculus (house mouse)
DOID:13514
  • venous tributary occlusion of retina
  • Aliases:
    • Venous tributary (branch) occlusion of retina
    • Venous tributary branch occlusion of retina
Mus musculus (house mouse)
DOID:0110350
  • osteogenesis imperfecta type 6
  • Aliases:
    • OI6
    • osteogenesis imperfecta type VI
Mus musculus (house mouse)
DOID:0090136
  • complex cortical dysplasia with other brain malformations 6
  • Aliases:
    • CDCBM56
Homo sapiens (human)
DOID:0112242
  • congenital symmetric circumferential skin creases 1
  • Aliases:
    • CSCSC1
Homo sapiens (human)
DOID:4617
  • periapical granuloma
  • Aliases:
    • Apical granuloma
Mus musculus (house mouse)
DOID:9507
  • ethmoid sinusitis
  • Aliases:
    • ethmoidal sinusitis
    • ethmoiditis
Mus musculus (house mouse)
DOID:6652
  • diffuse idiopathic skeletal hyperostosis
  • Aliases:
    • Ankylosing vertebral hyperostosis
    • DISH
    • Disseminated idiopathic skeletal hyperostosis
Homo sapiens (human)
DOID:9446
  • cholangitis
Mus musculus (house mouse)
DOID:10533
  • viral pneumonia
Mus musculus (house mouse)
DOID:0080390
  • nephrotic syndrome type 1
  • Aliases:
    • Finnish congenital nephrosis
Mus musculus (house mouse)
DOID:1063
  • interstitial nephritis
  • Aliases:
    • renal tubulo-interstitial disease
Mus musculus (house mouse)
DOID:0080528
  • bronchiectasis 3
Mus musculus (house mouse)
DOID:0060854
  • autosomal recessive pseudohypoaldosteronism type 1
  • Aliases:
    • PHA1B
    • autosomal recessive PHA 1
Mus musculus (house mouse)
DOID:0080527
  • bronchiectasis 2
Mus musculus (house mouse)
DOID:4479
  • pseudohypoaldosteronism
Mus musculus (house mouse)
DOID:0081118
  • benign familial infantile seizures 5
  • Aliases:
    • Benign Familial Infantile Seizures, 5
Mus musculus (house mouse)
DOID:0080445
  • developmental and epileptic encephalopathy 13
  • Aliases:
    • DEE13
    • early infantile epileptic encephalopathy 13
Mus musculus (house mouse)
DOID:0111074
  • progressive familial heart block type IA
  • Aliases:
    • PFHB1A
Mus musculus (house mouse)
DOID:0110218
  • Brugada syndrome 1
  • Aliases:
    • BRGDA1
Mus musculus (house mouse)
DOID:0110646
  • long QT syndrome 3
  • Aliases:
    • LQT3
Mus musculus (house mouse)
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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