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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 6151 - 6175 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲ Source
DOID:0110759
  • type 1 diabetes mellitus 22
  • Aliases:
    • IDDM22
    • Insulin-Dependent Diabetes Mellitus 22
Homo sapiens (human)
DOID:0050745
  • diffuse large B-cell lymphoma
  • Aliases:
    • DLBCL
Homo sapiens (human)
DOID:1856
  • cherubism
Homo sapiens (human)
DOID:2366
  • West Nile fever
Homo sapiens (human)
DOID:0110827
  • Usher syndrome type 2
  • Aliases:
    • USH2
Homo sapiens (human)
DOID:0080588
  • agammaglobulinemia 5
Homo sapiens (human)
DOID:1496
  • echinococcosis
  • Aliases:
    • Echinococcosis of liver
    • echinococcal disease
    • hepatic echinococcosis
    • hydatid disease
    • hydatidosis
    • liver echinococcus
    • pulmonary echinococcosis
Homo sapiens (human)
DOID:0060647
  • fetal encasement syndrome
  • Aliases:
    • cocoon syndrome
Homo sapiens (human)
DOID:0110521
  • autosomal recessive nonsyndromic deafness 70
  • Aliases:
    • DFNB70
    • autosomal recessive deafness 70
Homo sapiens (human)
DOID:0081046
  • frontonasal dysplasia 2
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
Homo sapiens (human)
DOID:0112321
  • alacrima, achalasia, and impaired intellectual development syndrome
  • Aliases:
    • AAMR
    • alacrima, achalasia, and mental retardation syndrome
Homo sapiens (human)
DOID:0111605
  • distal arthrogryposis type 2A
  • Aliases:
    • DA2A
    • distal arthrogryposis type 2A (Freeman-Sheldon)
Homo sapiens (human)
DOID:0050663
  • Bethlem myopathy
  • Aliases:
    • benign congenital muscular dystrophy
Homo sapiens (human)
DOID:0080821
  • exercise-induced bronchoconstriction
  • Aliases:
    • exercise-induced asthma
Homo sapiens (human)
DOID:13450
  • coccidioidomycosis
  • Aliases:
    • primary extrapulmonary coccidioidomycosis
Homo sapiens (human)
DOID:0060931
  • developmental dysplasia of the hip 1
  • Aliases:
    • DDH1
Homo sapiens (human)
DOID:14069
  • cerebral malaria
  • Aliases:
    • Malarial encephalitis
Homo sapiens (human)
DOID:0080948
  • agenesis of corpus callosum, cardiac, ocular, and genital syndrome
Homo sapiens (human)
DOID:0110661
  • congenital myasthenic syndrome 20
  • Aliases:
    • CMS20
    • congenital myasthenic syndrome 20 presynaptic
Homo sapiens (human)
DOID:0070050
  • neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language
  • Aliases:
    • MRD20
    • autosomal dominant mental retardation 20
    • mental retardation, autosomal dominant 20
Homo sapiens (human)
DOID:0060486
  • Perry syndrome
  • Aliases:
    • parkinsonism with alveolar hypoventilation and mental depression
Homo sapiens (human)
DOID:10460
  • nasopharyngitis
  • Aliases:
    • chronic nasopharyngitis
Homo sapiens (human)
DOID:2810
  • middle lobe syndrome
Homo sapiens (human)
DOID:0081221
  • autosomal recessive intellectual developmental disorder 59
Homo sapiens (human)
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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