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 8501 - 8525 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲ Source
DOID:0110019
  • age related macular degeneration 7
  • Aliases:
    • ARMD7
Mus musculus (house mouse)
DOID:10914
  • amnestic disorder
  • Aliases:
    • Amnestic syndrome
    • Korsakoff's psychosis or syndrome
    • amnesia
Mus musculus (house mouse)
DOID:0080839
  • X-linked warfarin sensitivity
Mus musculus (house mouse)
DOID:0110567
  • autosomal dominant nonsyndromic deafness 41
  • Aliases:
    • DFNA41
    • autosomal dominant deafness 41
Mus musculus (house mouse)
DOID:234
  • colon adenocarcinoma
  • Aliases:
    • Colonic adenocarcinoma
    • adenocarcinoma of colon
Mus musculus (house mouse)
DOID:635
  • acquired immunodeficiency syndrome
  • Aliases:
    • AIDS
    • acquired Immune deficiency
Mus musculus (house mouse)
DOID:0080501
  • GM1 gangliosidosis type 2
  • Aliases:
    • juvenile GM1 gangliosidosis
Mus musculus (house mouse)
DOID:0050561
  • Lennox-Gastaut syndrome
  • Aliases:
    • Lennox syndrome
Mus musculus (house mouse)
DOID:0112050
  • non-syndromic X-linked intellectual disability 63
  • Aliases:
    • ACSL4-related intellectual disability
    • MRX63
    • MRX68
    • X-linked mental retardation 63
    • X-linked mental retardation 68
Mus musculus (house mouse)
DOID:0110969
  • brachydactyly type B1
  • Aliases:
    • BDB1
Mus musculus (house mouse)
DOID:0080421
  • developmental and epileptic encephalopathy 11
  • Aliases:
    • DEE11
    • early infantile epileptic encephalopathy 11
Mus musculus (house mouse)
DOID:3525
  • middle cerebral artery infarction
Mus musculus (house mouse)
DOID:0070151
  • hereditary sensory and autonomic neuropathy type 6
  • Aliases:
    • HSAN6
    • hereditary sensory and autonomic neuropathy type VI
Mus musculus (house mouse)
DOID:0060327
  • omphalocele
  • Aliases:
    • omphalocoele
Mus musculus (house mouse)
DOID:0050450
  • Gitelman syndrome
  • Aliases:
    • HYPOMAGNESEMIA-HYPOKALEMIA, PRIMARY RENOTUBULAR, WITH HYPOCALCIURIA
Mus musculus (house mouse)
DOID:14179
  • X-linked agammaglobulinemia
  • Aliases:
    • BTK deficiency
    • Bruton agammaglobulinemia tyrosine kinase deficiency
    • Bruton disease
    • Bruton's Sex-Linked Agammaglobulinemia
    • Bruton's agammaglobulinaemia
    • Bruton's type agammaglobulinemia
    • Bruton-type agammaglobulinemia
Mus musculus (house mouse)
DOID:0090003
  • agenesis of the corpus callosum with peripheral neuropathy
  • Aliases:
    • Andermann syndrome
    • Charlevoix disease
    • corpus callosum agenesis-neuronopathy syndrome
Mus musculus (house mouse)
DOID:0111210
  • autosomal dominant distal hereditary motor neuronopathy 6
  • Aliases:
    • HMN IID
    • HMN2D
    • distal hereditary motor neuronopathy type 2D
    • distal hereditary motor neuropathy type IID
    • distal spinal muscular atrophy with calf predominance
Mus musculus (house mouse)
DOID:3877
  • functional colonic disease
Mus musculus (house mouse)
DOID:2236
  • congenital afibrinogenemia
  • Aliases:
    • Factor I deficiency
    • Fibrinogen deficiency
Mus musculus (house mouse)
DOID:4866
  • salivary gland adenoid cystic carcinoma
  • Aliases:
    • Cylindroma
Mus musculus (house mouse)
DOID:11396
  • pulmonary edema
Mus musculus (house mouse)
DOID:0111539
  • parastremmatic dwarfism
  • Aliases:
    • parastremmatic dysplasia
Mus musculus (house mouse)
DOID:0080390
  • nephrotic syndrome type 1
  • Aliases:
    • Finnish congenital nephrosis
Mus musculus (house mouse)
DOID:0110374
  • retinitis pigmentosa 68
  • Aliases:
    • RP68
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