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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 4526 - 4550 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0110909
  • inflammatory bowel disease 25
  • Aliases:
    • IBD25
    • early onset autosomal recessive inflammatory bowel disease 25
Homo sapiens (human)
DOID:12030
  • panuveitis
  • Aliases:
    • Diffuse uveitis
Mus musculus (house mouse)
DOID:0081082
  • acute myelomonocytic leukemia
Caenorhabditis elegans
DOID:0080855
  • Parkinsonism
Xenopus tropicalis (tropical clawed frog)
DOID:12132
  • granulomatosis with polyangiitis
  • Aliases:
    • Necrotizing respiratory granulomatosis
    • Wegener granulomatosis, formerly
Mus musculus (house mouse)
DOID:0112262
  • leucine-sensitive hypoglycemia of infancy
  • Aliases:
    • LIH
    • leucine-induced hypoglycemia
Mus musculus (house mouse)
DOID:0050557
  • congenital muscular dystrophy
Homo sapiens (human)
DOID:14557
  • primary pulmonary hypertension
  • Aliases:
    • Idiopathic pulmonary arterial hypertension
Drosophila melanogaster (fruit fly)
DOID:0110158
  • Charcot-Marie-Tooth disease type 2I
  • Aliases:
    • CMT2I
    • Charcot-Marie-Tooth neuropathy type 2I
Rattus norvegicus (Norway rat)
DOID:0111237
  • congenital muscular dystrophy-dystroglycanopathy type A1
  • Aliases:
    • MDDGA1
    • Walker-Warburg syndrome or muscle-eye-brain disease, POMT1-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A1
Xenopus tropicalis (tropical clawed frog)
DOID:0111478
  • combined oxidative phosphorylation deficiency 20
  • Aliases:
    • COXPD20
Homo sapiens (human)
DOID:4029
  • gastritis
  • Aliases:
    • Erosive Gastritis
    • Erosive gastropathy
    • acute gastric mucosal erosion
Mus musculus (house mouse)
DOID:869
  • cholesteatoma
Drosophila melanogaster (fruit fly)
DOID:0080319
  • X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia
  • Aliases:
    • XMEN
Danio rerio (zebrafish)
DOID:905
  • Zellweger syndrome
  • Aliases:
    • cerebrohepatorenal syndrome
    • congenital iron overload
Rattus norvegicus (Norway rat)
DOID:0060189
  • ileitis
  • Aliases:
    • Crohn's ileitis
Mus musculus (house mouse)
DOID:3369
  • Ewing sarcoma
  • Aliases:
    • Ewing's family localized tumor
    • Ewing's sarcoma/peripheral primitive neuroectodermal tumor
    • Ewing's tumor
    • Ewings sarcoma
    • Ewings sarcoma-primitive neuroectodermal tumor
    • PNET of Thoracopulmonary Region
    • localized Ewing sarcoma
    • localized Ewing's sarcoma
    • localized Ewing's sarcoma/peripheral primitive neuroectodermal tumor
    • localized Ewing's tumor
    • localized peripheral primitive neuroectodermal tumor
    • peripheral primitive neuroectodermal tumor
Mus musculus (house mouse)
DOID:12986
  • leukostasis
Homo sapiens (human)
DOID:0060852
  • Pierson syndrome
  • Aliases:
    • microcoria-congenital nephrosis syndrome
Homo sapiens (human)
DOID:0111403
  • mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations
  • Aliases:
    • MCCCHCM
Mus musculus (house mouse)
DOID:0112139
  • nuclear type mitochondrial complex I deficiency 35
  • Aliases:
    • MC1DN35
Rattus norvegicus (Norway rat)
DOID:0111732
  • Eiken syndrome
  • Aliases:
    • Eiken skeletal dysplasia
    • bone modeling defect of hands and feet
Caenorhabditis elegans
DOID:0081292
  • traumatic brain injury
Drosophila melanogaster (fruit fly)
DOID:6688
  • autoimmune lymphoproliferative syndrome
  • Aliases:
    • ALPS
    • Canale-Smith syndrome
Rattus norvegicus (Norway rat)
DOID:0060439
  • lysinuric protein intolerance
  • Aliases:
    • LPI
    • dibasic amino aciduria II
    • hyperdibasic aminoaciduria
Mus musculus (house mouse)
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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