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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 10376 - 10400 of 15957 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:0080339
  • familial erythrocytosis 4
  • Aliases:
    • ECYT4
Homo sapiens (human)
DOID:14175
  • von Hippel-Lindau disease
  • Aliases:
    • Hippel Lindau syndrome
    • von Hippel-Lindau syndrome
Homo sapiens (human)
DOID:705
  • Leber hereditary optic neuropathy
  • Aliases:
    • Leber's hereditary optic neuropathy
    • Leber's optic atrophy
Saccharomyces cerevisiae S288C
DOID:0080060
  • autosomal recessive spinocerebellar ataxia 12
  • Aliases:
    • SCAR12
Saccharomyces cerevisiae S288C
DOID:0080452
  • developmental and epileptic encephalopathy 28
  • Aliases:
    • DEE28
    • early infantile epileptic encephalopathy 28
Saccharomyces cerevisiae S288C
DOID:0110330
  • Leber congenital amaurosis 13
  • Aliases:
    • LCA13
Saccharomyces cerevisiae S288C
DOID:1749
  • squamous cell carcinoma
  • Aliases:
    • epidermoid carcinoma
    • malignant squamous cell tumor
    • squamous carcinoma
    • squamous cell Epithelioma
    • squamous cell cancer
Saccharomyces cerevisiae S288C
DOID:14791
  • Leber congenital amaurosis
  • Aliases:
    • LCA
    • Leber's amaurosis
    • Leber's congenital amaurosis
    • Leber's disease
Saccharomyces cerevisiae S288C
DOID:0110815
  • hereditary spastic paraplegia 64
  • Aliases:
    • SPG64
    • autosomal recessive spastic paraplegia 64
    • autosomal recessive spastic paraplegia type 64
Homo sapiens (human)
DOID:0080333
  • aortic valve disease 1
Homo sapiens (human)
DOID:1800
  • neuroendocrine carcinoma
Homo sapiens (human)
DOID:12783
  • migraine without aura
  • Aliases:
    • common migraine
Homo sapiens (human)
DOID:12783
  • migraine without aura
  • Aliases:
    • common migraine
Saccharomyces cerevisiae S288C
DOID:1800
  • neuroendocrine carcinoma
Saccharomyces cerevisiae S288C
DOID:936
  • brain disease
  • Aliases:
    • encephalopathy
Saccharomyces cerevisiae S288C
DOID:11054
  • urinary bladder cancer
  • Aliases:
    • bladder cancer
    • tumor of the bladder
Saccharomyces cerevisiae S288C
DOID:1712
  • aortic valve stenosis
  • Aliases:
    • Aortic stenosis
    • Rheumatic aortic stenosis
    • rheumatic aortic valve stenosis
Saccharomyces cerevisiae S288C
DOID:14115
  • toxic shock syndrome
  • Aliases:
    • TSS
    • toxic shock
Saccharomyces cerevisiae S288C
DOID:0080855
  • Parkinsonism
Saccharomyces cerevisiae S288C
DOID:10652
  • Alzheimer's disease
  • Aliases:
    • Alzheimer disease
    • Alzheimers dementia
Saccharomyces cerevisiae S288C
DOID:1037
  • lymphoid leukemia
  • Aliases:
    • lymphoblastic leukaemia
    • lymphoblastic leukemia
    • lymphocytic leukaemia
Homo sapiens (human)
DOID:0110052
  • amelogenesis imperfecta type 1B
  • Aliases:
    • AI1B
    • AIH2
    • amelogenesis imperfecta type IB
    • autosomal dominant hypoplastic local amelogenesis imperfecta
    • hereditary localized enamel hypoplasia
Homo sapiens (human)
DOID:0110056
  • amelogenesis imperfecta type 1C
  • Aliases:
    • AI1C
    • amelogenesis imperfecta type IC
    • autosomal recessive amelogenesis imperfecta hypoplastic with or without openbite malocclusion
    • autosomal recessive amelogenesis imperfecta local hypoplastic type
Homo sapiens (human)
DOID:0080386
  • nephrotic syndrome type 10
Homo sapiens (human)
DOID:0081399
  • autosomal dominant distal hereditary motor neuronopathy 10
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