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 1676 - 1700 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:0060752
  • familial temporal lobe epilepsy 5
  • Aliases:
    • ETL5
Saccharomyces cerevisiae S288C
DOID:0110847
  • xeroderma pigmentosum variant type
  • Aliases:
    • XPV
    • photosensitivity with defective DNA synthesis
    • xeroderma pigmentosum with normal DNA repair rates
Saccharomyces cerevisiae S288C
DOID:14067
  • Plasmodium falciparum malaria
  • Aliases:
    • Malaria fever, subtertian
    • falciparum malaria
    • malignant tertian fever
Saccharomyces cerevisiae S288C
DOID:8577
  • ulcerative colitis
  • Aliases:
    • Left-sided ulcerative colitis
Saccharomyces cerevisiae S288C
DOID:9563
  • bronchiectasis
  • Aliases:
    • Polynesian bronchiectasis
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:0110555
  • autosomal dominant nonsyndromic deafness 25
  • Aliases:
    • DFNA25
    • autosomal dominant deafness 25
Saccharomyces cerevisiae S288C
DOID:13406
  • pulmonary sarcoidosis
  • Aliases:
    • lung Sarcoidosis
Saccharomyces cerevisiae S288C
DOID:11721
  • glycogen storage disease VII
  • Aliases:
    • Glycogen storage disease 7
    • Glycogen storage disease, type VII
    • Muscle phosphofructokinase deficiency
    • glycogen storage disease type VII
    • phosphofructokinase myopathy
Saccharomyces cerevisiae S288C
DOID:0050577
  • cranioectodermal dysplasia
  • Aliases:
    • Levin syndrome
    • Sensenbrenner syndrome
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:178
  • vascular disease
  • Aliases:
    • vascular tissue disease
Saccharomyces cerevisiae S288C
DOID:3659
  • sialuria
Saccharomyces cerevisiae S288C
DOID:1852
  • intrahepatic cholestasis
  • Aliases:
    • neonatal intrahepatic cholestasis
Saccharomyces cerevisiae S288C
DOID:5844
  • myocardial infarction
  • Aliases:
    • Myocardial infarct
    • heart attack
Saccharomyces cerevisiae S288C
DOID:0050797
  • peroxisomal acyl-CoA oxidase deficiency
  • Aliases:
    • Peroxisomal acyl-coenzyme A oxidase
Saccharomyces cerevisiae S288C
DOID:0060448
  • Fleck corneal dystrophy
  • Aliases:
    • FCD
    • Francois-Neetens speckled corneal dystrophy
Saccharomyces cerevisiae S288C
DOID:8557
  • oropharynx cancer
  • Aliases:
    • Oropharyngeal carcinoma
    • malignant Oropharyngeal tumor
    • malignant tumor of oropharynx
    • malignant tumour of mesopharynx
    • oropharyngeal cancer
Saccharomyces cerevisiae S288C
DOID:251
  • alcohol-induced mental disorder
Saccharomyces cerevisiae S288C
DOID:13375
  • temporal arteritis
  • Aliases:
    • Horton's disease
    • giant cell arteritis
Saccharomyces cerevisiae S288C
DOID:1824
  • status epilepticus
  • Aliases:
    • Grand mal status
Saccharomyces cerevisiae S288C
DOID:0111668
  • Kohlschutter-Tonz syndrome
  • Aliases:
    • KTZS
    • Kohlschutter's syndrome
    • amelocerebrohypohidrotic syndrome
    • epilepsy and yellow teeth
    • epilepsy dementia amelogenesis imperfecta
    • epilepsy-dementia-amelogenesis imperfecta syndrome
Saccharomyces cerevisiae S288C
DOID:0090044
  • dystonia 9
Saccharomyces cerevisiae S288C
DOID:10754
  • otitis media
Saccharomyces cerevisiae S288C
DOID:0112182
  • mismatch repair cancer syndrome
  • Aliases:
    • BTP1 syndrome
    • BTPS1
    • CMMR-D syndrome
    • CMMRDS
    • MMR deficiency
    • Turcot syndrome
    • brain tumor-polyposis syndrome 1
    • childhood cancer syndrome
    • constitutional mismatch repair deficiency syndrome
Saccharomyces cerevisiae S288C

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Last updated: December 9, 2024