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 1801 - 1825 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:0060001
  • withdrawal disorder
Saccharomyces cerevisiae S288C
DOID:0070376
  • developmental and epileptic encephalopathy 31B
  • Aliases:
    • DEE31B
Saccharomyces cerevisiae S288C
DOID:3748
  • esophagus squamous cell carcinoma
  • Aliases:
    • SCC of esophagus
    • SCC of oesophagus
    • oesophagus squamous cell carcinoma
Saccharomyces cerevisiae S288C
DOID:0111864
  • autosomal recessive congenital bilateral absence of vas deferens
Saccharomyces cerevisiae S288C
DOID:2566
  • corneal dystrophy
Saccharomyces cerevisiae S288C
DOID:1059
  • intellectual disability
Saccharomyces cerevisiae S288C
DOID:5410
  • pulmonary neuroendocrine tumor
Saccharomyces cerevisiae S288C
DOID:0080377
  • peroxisomal biogenesis disorder
Saccharomyces cerevisiae S288C
DOID:0080530
  • granular corneal dystrophy 1
  • Aliases:
    • corneal dystrophy, Groenouw type I
Saccharomyces cerevisiae S288C
DOID:0080560
  • congenital disorder of glycosylation Ih
  • Aliases:
    • congenital disorder of glycosylation 1h
Saccharomyces cerevisiae S288C
DOID:0111240
  • congenital muscular dystrophy-dystroglycanopathy type A2
  • Aliases:
    • MDDGA2
    • Walker-Warburg syndrome or muscle-eye-brain disease, POMT2-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A2
Saccharomyces cerevisiae S288C
DOID:10595
  • Charcot-Marie-Tooth disease
  • Aliases:
    • CMT - Charcot-Marie-Tooth disease
Saccharomyces cerevisiae S288C
DOID:0112056
  • X-linked intellectual disability-short stature-overweight syndrome
  • Aliases:
    • MRX12
    • MRX35
    • X-linked mental retardation 12
    • X-linked mental retardation 35
Saccharomyces cerevisiae S288C
DOID:0112218
  • developmental and epileptic encephalopathy 83
  • Aliases:
    • DEE83
    • early infantile epileptic encephalopathy 83
Saccharomyces cerevisiae S288C
DOID:0081133
  • 3-methylglutaconic aciduria type 7a
Saccharomyces cerevisiae S288C
DOID:0070400
  • hypomyelinating leukodystrophy 19
  • Aliases:
    • HLD19
Saccharomyces cerevisiae S288C
DOID:10881
  • hand, foot and mouth disease
  • Aliases:
    • Vesicular stomatitis and exanthem
Saccharomyces cerevisiae S288C
DOID:0110255
  • cataract 5 multiple types
  • Aliases:
    • CTRCT5
Saccharomyces cerevisiae S288C
DOID:14717
  • centronuclear myopathy
  • Aliases:
    • myotubular myopathy
Saccharomyces cerevisiae S288C
DOID:0111698
  • proprotein convertase 1/3 deficiency
  • Aliases:
    • PCI deficiency
    • obesity and endocrinopathy due to impaired processing of prohormones
    • obesity due to prohormone convertase I deficiency
    • obesity with impaired prohormone processing
Saccharomyces cerevisiae S288C
DOID:0060759
  • immunodeficiency with hyper IgM type 5
  • Aliases:
    • HIGM5
    • hyper-IgM syndrome 5
    • hyper-IgM syndrome due to UNG deficiency
    • hyper-IgM syndrome due to uracil N-glycosylase
Saccharomyces cerevisiae S288C
DOID:299
  • adenocarcinoma
Saccharomyces cerevisiae S288C
DOID:0112189
  • thyroid dyshormonogenesis 6
  • Aliases:
    • TDH6
    • genetic defect in thyroid hormonogenesis 6
Rattus norvegicus (Norway rat)
DOID:5223
  • infertility
Rattus norvegicus (Norway rat)
DOID:9538
  • multiple myeloma
  • Aliases:
    • myeloma
Rattus norvegicus (Norway rat)

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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