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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 14451 - 14475 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0070341
  • neonatal-onset type II citrullinemia
  • Aliases:
    • neonatal-onset type 2 citrullinemia
Mus musculus (house mouse)
DOID:4948
  • gallbladder carcinoma
  • Aliases:
    • cancer of the gallbladder
    • carcinoma gallbladder
    • carcinoma of gallbladder
Caenorhabditis elegans
DOID:3978
  • extrinsic cardiomyopathy
Caenorhabditis elegans
DOID:0111809
  • syndromic microphthalmia 2
  • Aliases:
    • ANOP2
    • MAA2
    • MCOPS2
    • OFCD syndrome
    • cataract-microphthalmia-radiculomegaly-cardiac septal defect syndrome
    • microphthalmia cataracts radiculomegaly and septal heart defects
    • oculofaciocardiodental syndrome
    • syndromic microphthalmia type 2
Mus musculus (house mouse)
DOID:1929
  • supravalvular aortic stenosis
  • Aliases:
    • Supra-valvular aortic stenosis
Mus musculus (house mouse)
DOID:0060577
  • 3MC syndrome 3
Homo sapiens (human)
DOID:0050881
  • inclusion body myopathy with Paget disease of bone and frontotemporal dementia
  • Aliases:
    • IBMPFD
    • inclusion body myopathy with Paget's disease of bone and frontotemporal dementia
Rattus norvegicus (Norway rat)
DOID:1727
  • retinal vein occlusion
  • Aliases:
    • Occlusion, of retinal vein
Rattus norvegicus (Norway rat)
DOID:14791
  • Leber congenital amaurosis
  • Aliases:
    • LCA
    • Leber's amaurosis
    • Leber's congenital amaurosis
    • Leber's disease
Drosophila melanogaster (fruit fly)
DOID:14452
  • hypokalemic periodic paralysis
  • Aliases:
    • Hypokalemic familial periodic paralysis
    • Periodic paralysis I
    • Westphal disease
    • familial hypokalemic periodic paralysis
    • periodic hypokalemic paralysis
Caenorhabditis elegans
DOID:1827
  • idiopathic generalized epilepsy
  • Aliases:
    • Generalised epilepsy
Drosophila melanogaster (fruit fly)
DOID:4535
  • hypotrichosis
Homo sapiens (human)
DOID:0060299
  • complement component 6 deficiency
Homo sapiens (human)
DOID:3410
  • carotid artery thrombosis
Mus musculus (house mouse)
DOID:7147
  • ankylosing spondylitis
  • Aliases:
    • Bekhterev syndrome
    • Bekhterev's disease
    • Marie-Strumpell disease
Rattus norvegicus (Norway rat)
DOID:0111223
  • centronuclear myopathy 1
  • Aliases:
    • CNM1
Rattus norvegicus (Norway rat)
DOID:0111458
  • galactose epimerase deficiency
  • Aliases:
    • GALE deficiency
    • GALE-D
    • UDP-galactose-4-epimerase deficiency
    • epimerase deficiency galactosemia
    • galactosemia III
    • galactosemia type 3
    • uridine diphosphate galactose-4-epimerase deficiency
Caenorhabditis elegans
DOID:0111909
  • autosomal dominant thrombophilia due to protein C deficiency
  • Aliases:
    • THPH3
    • autosomal dominant PROC deficiency
    • autosomal dominant protein C deficiency
Mus musculus (house mouse)
DOID:12510
  • retinal ischemia
Danio rerio (zebrafish)
DOID:10754
  • otitis media
Homo sapiens (human)
DOID:0050771
  • pheochromocytoma
  • Aliases:
    • phaeochromocytoma
Caenorhabditis elegans
DOID:2841
  • asthma
  • Aliases:
    • bronchial hyperreactivity
    • chronic obstructive asthma
    • chronic obstructive asthma with acute exacerbation
    • chronic obstructive asthma with status asthmaticus
Drosophila melanogaster (fruit fly)
DOID:0070482
  • spinal neurofibromatosis
  • Aliases:
    • FNSF
    • SNF
    • familial spinal neurofibromatosis
Homo sapiens (human)
DOID:0060036
  • intrinsic cardiomyopathy
Mus musculus (house mouse)
DOID:1849
  • cannabis dependence
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