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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 14501 - 14525 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0060409
  • NFIA-related disorder
  • Aliases:
    • 1p31p32 microdeletion syndrome
    • Chromosome 1, Monosomy 1p32
    • brain malformations with or without urinary tract defects
    • chromosome 1p32-p31 deletion syndrome
Homo sapiens (human)
DOID:0050904
  • salivary gland carcinoma
Danio rerio (zebrafish)
DOID:8893
  • psoriasis
Drosophila melanogaster (fruit fly)
DOID:11168
  • anogenital venereal wart
  • Aliases:
    • Anogenital Human papilloma Virus Infectious Disease
    • Anogenital warts
    • Genital warts
    • genital wart virus infectious disease
    • venereal wart
Rattus norvegicus (Norway rat)
DOID:2216
  • factor V deficiency
  • Aliases:
    • Hereditary hypoproaccelerinaemia
    • Labile factor deficiency
    • Proaccelerin deficiency
    • deficiency, labile
Mus musculus (house mouse)
DOID:0110770
  • hereditary spastic paraplegia 17
  • Aliases:
    • SPG17
    • Silver spastic paraplegia syndrome
    • Silver syndrome
    • autosomal dominant spastic paraplegia 17
    • autosomal dominant spastic paraplegia type 17
    • dHMN5B
    • distal hereditary motor neuropathy type 5B
    • spastic paraplegia with amyotrophy of hands and feet
    • spastic paraplegia-amyotrophy of hands and feet
Rattus norvegicus (Norway rat)
DOID:0060652
  • familial erythrocytosis 1
  • Aliases:
    • ECYT1
    • autosomal dominant benign erythrocytosis
    • primary familial and congenital polycythemia
Xenopus laevis (African clawed frog)
DOID:0060879
  • primary hypomagnesemia
  • Aliases:
    • HOMG
    • primary familial hypomagnesemia
Rattus norvegicus (Norway rat)
DOID:0110219
  • Brugada syndrome 2
  • Aliases:
    • BRGDA2
Saccharomyces cerevisiae S288C
DOID:417
  • autoimmune disease
  • Aliases:
    • autoimmune hypersensitivity disease
    • hypersensitivity reaction type II disease
Rattus norvegicus (Norway rat)
DOID:1681
  • heart septal defect
  • Aliases:
    • Cardiac septal defects
    • Congenital septal defect of heart
    • septal defect
Mus musculus (house mouse)
DOID:0050852
  • limb ischemia
Drosophila melanogaster (fruit fly)
DOID:8955
  • sideroblastic anemia
  • Aliases:
    • ANEMIA SIDEROBLASTIC
    • Anemia, hypochromic with iron loading
Homo sapiens (human)
DOID:0050697
  • chorioamnionitis
Caenorhabditis elegans
DOID:0112306
  • Mahvash Disease
  • Aliases:
    • GCGR-related hyperglucagonemia
    • nesidioblastosis, alpha cell hyperplasia, microglucagonoma, and nonfunctioning islet cell tumor
Mus musculus (house mouse)
DOID:0050456
  • Buruli ulcer disease
  • Aliases:
    • Bairnsdale ulcer
    • Daintree ulcer
    • Mossman ulcer
    • Searl ulcer
    • Searle's ulcer
Rattus norvegicus (Norway rat)
DOID:0060676
  • catecholaminergic polymorphic ventricular tachycardia 2
  • Aliases:
    • CVPT2
Caenorhabditis elegans
DOID:0111052
  • Scott syndrome
  • Aliases:
    • BDPLT7
    • SCTS
    • bleeding abnormality due to deficiency of platelet biding of factor X
    • familial prothrombin consumption inhibitor
    • familial prothrombin conversion defect
    • platelet-type bleeding disorder 7
    • prothrombin consumption deficiency
Homo sapiens (human)
DOID:11984
  • hypertrophic cardiomyopathy
  • Aliases:
    • hypertrophic obstructive cardiomyopathy
Drosophila melanogaster (fruit fly)
DOID:0111558
  • Charcot-Marie-Tooth disease type 2DD
  • Aliases:
    • ATP1A1-related CMT2
    • ATP1A1-related autosomal dominant Charcot-Marie-Tooth disease type 2
    • CMT2DD
    • Charcot-Marie-Tooth disease, axonal, type 2DD
    • Charcot-Marie-Tooth neuropathy, type 2DD
Rattus norvegicus (Norway rat)
DOID:0070299
  • multiple epiphyseal dysplasia 5
  • Aliases:
    • BHMED
    • EDM5
    • bilateral hereditary microepiphyseal dysplasia
    • multiple epiphyseal dysplasia MATN3-related
Caenorhabditis elegans
DOID:0110342
  • osteogenesis imperfecta type 13
  • Aliases:
    • OI13
    • osteogenesis imperfecta type XIII
Mus musculus (house mouse)
DOID:0110682
  • congenital myasthenic syndrome 16
  • Aliases:
    • CMS16
    • congenital myasthenic syndrome acetazolamide-responsive
Homo sapiens (human)
DOID:1930
  • Laurence-Moon syndrome
  • Aliases:
    • LNMS
Homo sapiens (human)
DOID:0060730
  • torsion dystonia 1
  • Aliases:
    • dystonia musculorum deformans
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