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 10251 - 10275 of 15957 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:0060879
  • primary hypomagnesemia
  • Aliases:
    • HOMG
    • primary familial hypomagnesemia
Rattus norvegicus (Norway rat)
DOID:0050881
  • inclusion body myopathy with Paget disease of bone and frontotemporal dementia
  • Aliases:
    • IBMPFD
    • inclusion body myopathy with Paget's disease of bone and frontotemporal dementia
Rattus norvegicus (Norway rat)
DOID:3181
  • oligodendroglioma
  • Aliases:
    • oligodendroglial neoplasm
    • oligodendroglial tumor
Rattus norvegicus (Norway rat)
DOID:0050782
  • Zollinger-Ellison syndrome
Rattus norvegicus (Norway rat)
DOID:0060879
  • primary hypomagnesemia
  • Aliases:
    • HOMG
    • primary familial hypomagnesemia
Mus musculus (house mouse)
DOID:0060882
  • renal hypomagnesemia 4
  • Aliases:
    • HOMG4
Mus musculus (house mouse)
DOID:3181
  • oligodendroglioma
  • Aliases:
    • oligodendroglial neoplasm
    • oligodendroglial tumor
Mus musculus (house mouse)
DOID:0050881
  • inclusion body myopathy with Paget disease of bone and frontotemporal dementia
  • Aliases:
    • IBMPFD
    • inclusion body myopathy with Paget's disease of bone and frontotemporal dementia
Mus musculus (house mouse)
DOID:0050782
  • Zollinger-Ellison syndrome
Mus musculus (house mouse)
DOID:10485
  • esophageal atresia
  • Aliases:
    • Congenital atresia of esophagus
    • Congenital imperforate esophagus
    • Imperforate esophagus
    • Oesophageal atresia
Mus musculus (house mouse)
DOID:0080196
  • mandibulofacial dysostosis, Guion-Almeida type
  • Aliases:
    • MFDM syndrome
    • mandibulofacial dysostosis with microcephaly
    • mandibulofacial dysostosis-microcephaly syndrome
Mus musculus (house mouse)
DOID:2908
  • Treacher Collins syndrome
  • Aliases:
    • Franceschetti syndrome
    • mandibulofacial dysostosis
Mus musculus (house mouse)
DOID:14737
  • craniofrontonasal syndrome
  • Aliases:
    • CFND
    • CFNS
    • craniofrontonasal dysostosis
    • craniofrontonasal dysplasia
Mus musculus (house mouse)
DOID:1934
  • dysostosis
Mus musculus (house mouse)
DOID:0060668
  • anencephaly
Mus musculus (house mouse)
DOID:0060668
  • anencephaly
Rattus norvegicus (Norway rat)
DOID:0050645
  • arterial tortuosity syndrome
Mus musculus (house mouse)
DOID:0070133
  • autosomal recessive cutis laxa type IB
  • Aliases:
    • ARCL1B
Mus musculus (house mouse)
DOID:3376
  • bone osteosarcoma
  • Aliases:
    • Osteosarcoma of bone
    • primary Osteosarcoma of bone
Mus musculus (house mouse)
DOID:0060745
  • Doyne honeycomb retinal dystrophy
  • Aliases:
    • DHRD
    • Doyne honeycomb degeneration of retina
Mus musculus (house mouse)
DOID:657
  • adenoma
  • Aliases:
    • acinar cell adenoma
    • acinic cell adenoma
    • adenomas
Mus musculus (house mouse)
DOID:0050975
  • spinocerebellar ataxia type 26
Mus musculus (house mouse)
DOID:3073
  • brain glioblastoma multiforme
  • Aliases:
    • Glioblastoma multiforme of brain
    • brain Glioblastoma
Mus musculus (house mouse)
DOID:1996
  • rectum adenocarcinoma
  • Aliases:
    • Rectal adenocarcinoma
Mus musculus (house mouse)
DOID:0070068
  • autosomal dominant intellectual developmental disorder 38
  • Aliases:
    • MRD38
    • PRELDS
    • autosomal dominant mental retardation 38
    • autosomal dominant non-syndromic intellectual disability 38
    • psychomotor retardation, epilepsy, and language disability syndrome
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