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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 1301 - 1325 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:5213
  • chronic inflammatory demyelinating polyradiculoneuropathy
Mus musculus (house mouse)
DOID:6196
  • reactive arthritis
  • Aliases:
    • Fiessinger Leroy Reiter syndrome
    • Post-bacterial arthropathy
    • Reiter disease
    • Reiter's disease
    • postdysenteric arthropathy
Homo sapiens (human)
DOID:331
  • central nervous system disease
Caenorhabditis elegans
DOID:799
  • varicose veins
  • Aliases:
    • Varix
    • Venous ectasia
    • Venous varices
    • varices
Drosophila melanogaster (fruit fly)
DOID:0110349
  • osteogenesis imperfecta type 9
  • Aliases:
    • OI9
    • osteogenesis imperfecta type IX
Saccharomyces cerevisiae S288C
DOID:0111651
  • ectodermal dysplasia 15
  • Aliases:
    • ECTD15
    • ectodermal dysplasia 15, hypohidrotic/hair type
Mus musculus (house mouse)
DOID:4543
  • retrograde amnesia
Mus musculus (house mouse)
DOID:9240
  • erythromelalgia
  • Aliases:
    • erythermalgia
Rattus norvegicus (Norway rat)
DOID:0110977
  • brachydactyly type A1C
  • Aliases:
    • BDA1C
Homo sapiens (human)
DOID:4608
  • common bile duct neoplasm
  • Aliases:
    • neoplasm of common bile duct
Danio rerio (zebrafish)
DOID:4154
  • dentinogenesis imperfecta
Rattus norvegicus (Norway rat)
DOID:445
  • Bartter disease
  • Aliases:
    • Aldosteronism with hyperplasia of the adrenal cortex
    • Bartter's syndrome
Homo sapiens (human)
DOID:0050083
  • Keshan disease
Mus musculus (house mouse)
DOID:0111234
  • congenital muscular dystrophy-dystroglycanopathy A7
  • Aliases:
    • MDDGA7
    • Walker-Warburg syndrome or muscle-eye-brain disease ISPD-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A7
Homo sapiens (human)
DOID:0111232
  • congenital muscular dystrophy-dystroglycanopathy type A9
  • Aliases:
    • MDDGA9
    • Walker-Warburg syndrome or muscle-eye-brain disease DAG1-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A9
Drosophila melanogaster (fruit fly)
DOID:37
  • skin disease
  • Aliases:
    • Genodermatosis
    • skin and subcutaneous tissue disease
Rattus norvegicus (Norway rat)
DOID:820
  • myocarditis
  • Aliases:
    • Myocardial inflammation
Danio rerio (zebrafish)
DOID:0111341
  • primary failure of tooth eruption
  • Aliases:
    • PFE
    • dental noneruption
    • familial posterior openbite malocclusion
    • nonsyndromic primary failure of eruption
    • primary retention of teeth
    • unerupted second primary molar
Homo sapiens (human)
DOID:0050547
  • familial medullary thyroid carcinoma
  • Aliases:
    • THYROID CARCINOMA, FAMILIAL MEDULLARY
Homo sapiens (human)
DOID:0111438
  • optic atrophy 5
  • Aliases:
    • OPA5
Homo sapiens (human)
DOID:0080507
  • Cornelia de Lange syndrome 3
  • Aliases:
    • CDLS3
    • Cornelia De Lange syndrome 3 with or without midline brain defects
Saccharomyces cerevisiae S288C
DOID:2526
  • prostate adenocarcinoma
Xenopus laevis (African clawed frog)
DOID:0090060
  • Wolcott-Rallison syndrome
Homo sapiens (human)
DOID:2377
  • multiple sclerosis
  • Aliases:
    • Generalized multiple sclerosis
    • insular sclerosis
Xenopus tropicalis (tropical clawed frog)
DOID:3891
  • placental insufficiency
Caenorhabditis elegans
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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