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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 10576 - 10600 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:4810
  • cerebrotendinous xanthomatosis
  • Aliases:
    • Cholestanol storage disease
Homo sapiens (human)
DOID:3049
  • Churg-Strauss syndrome
  • Aliases:
    • Allergic Granulomatous Angiitis
    • Allergic granulomatosis angiitis
    • Churg-Strauss vasculitis
Homo sapiens (human)
DOID:0110831
  • Usher syndrome type 1D
  • Aliases:
    • USH1D
    • Usher syndrome type ID
Homo sapiens (human)
DOID:6726
  • fibrillary astrocytoma
  • Aliases:
    • Fibrillary Astrocytic tumors
Homo sapiens (human)
DOID:0060849
  • osteoporosis-pseudoglioma syndrome
  • Aliases:
    • OPPG
    • ocular form of osteogenesis imperfecta
Homo sapiens (human)
DOID:0081371
  • lacrimoauriculodentodigital syndrome 2
  • Aliases:
    • Lacrimo-auriculo-dento-digital syndrome 2
Homo sapiens (human)
DOID:2526
  • prostate adenocarcinoma
Homo sapiens (human)
DOID:0090094
  • hypogonadotropic hypogonadism 1 with or without anosmia
  • Aliases:
    • dysplasia olfactogenitalis of de morsier
Homo sapiens (human)
DOID:0080425
  • developmental and epileptic encephalopathy 47
  • Aliases:
    • DEE47
    • early infantile epileptic encephalopathy 47
Homo sapiens (human)
DOID:0080922
  • bilateral frontoparietal polymicrogyria
Homo sapiens (human)
DOID:809
  • cocaine abuse
Homo sapiens (human)
DOID:0050990
  • episodic ataxia type 2
Homo sapiens (human)
DOID:0070380
  • developmental and epileptic encephalopathy 85
  • Aliases:
    • DEE85
    • early infantile epileptic encephalopathy 85
Homo sapiens (human)
DOID:0090076
  • hypogonadotropic hypogonadism 18 with or without anosmia
Homo sapiens (human)
DOID:0081443
  • Stolerman neurodevelopmental syndrome
Homo sapiens (human)
DOID:1056
  • oculocerebrorenal syndrome
  • Aliases:
    • Lowe syndrome
    • lowe oculocerebrorenal syndrome
    • oculocerebrorenal syndrome of Lowe
Homo sapiens (human)
DOID:0070490
  • infantile parkinsonism-dystonia 2
  • Aliases:
    • Brain dopamine-serotonin vesicular transport disease
    • PKDYS2
Homo sapiens (human)
DOID:0060023
  • immunodeficiency with hyper IgM type 3
  • Aliases:
    • CD40 deficiency
    • HIGM3
    • hyper-IgM syndrome due to CD40 deficiency
    • type 3 hyper-IgM immunodeficiency
Homo sapiens (human)
DOID:628
  • combined T cell and B cell immunodeficiency
  • Aliases:
    • Congenital Combined Immunodeficiency
Homo sapiens (human)
DOID:4249
  • Gerstmann-Straussler-Scheinker syndrome
  • Aliases:
    • Gerstmann-Straussler-Scheinker disease
    • PRION DEMENTIA
Homo sapiens (human)
DOID:9975
  • cocaine dependence
Homo sapiens (human)
DOID:0110225
  • Brugada syndrome 8
  • Aliases:
    • BRGDA8
Homo sapiens (human)
DOID:0070219
  • familial hyperinsulinemic hypoglycemia 1
  • Aliases:
    • HHF1
Homo sapiens (human)
DOID:2772
  • irritant dermatitis
  • Aliases:
    • irritant contact dermatitis
    • primary irritant dermatitis
Homo sapiens (human)
DOID:0111100
  • maturity-onset diabetes of the young type 2
  • Aliases:
    • MODY glucokinase-related
    • MODY type 2
    • MODY2
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