GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 3701 - 3725 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:12894
  • Sjogren's syndrome
  • Aliases:
    • Sicca syndrome
    • Sjogren syndrome
    • xerodermosteosis
Homo sapiens (human)
DOID:899
  • choledochal cyst
  • Aliases:
    • Congenital choledochal cyst
    • bile duct cyst
    • biliary cyst
Homo sapiens (human)
DOID:12704
  • ataxia telangiectasia
  • Aliases:
    • Boder-Sedgwick syndrome
    • Louis Bar syndrome
Homo sapiens (human)
DOID:8866
  • actinic keratosis
  • Aliases:
    • SK - Solar keratosis
    • Senile hyperkeratosis
    • Solar keratosis
    • actinic (Solar) Keratosis
Homo sapiens (human)
DOID:0080190
  • malignant epithelioid hemangioendothelioma
Homo sapiens (human)
DOID:0111070
  • congenital bile acid synthesis defect 3
  • Aliases:
    • CBAS3
    • oxysterol 7-alpha-hydroxylase deficiency
Homo sapiens (human)
DOID:0110774
  • hereditary spastic paraplegia 23
  • Aliases:
    • Lison syndrome
    • SPG23
    • Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome
    • spastic paraplegia 23
    • spastic paraplegia with pigmentary abnormalities
Homo sapiens (human)
DOID:7305
  • astroblastoma
Homo sapiens (human)
DOID:3234
  • central nervous system lymphoma
  • Aliases:
    • Microglioma
    • primary CNS lymphoma
Homo sapiens (human)
DOID:593
  • agoraphobia
  • Aliases:
    • Fear of open spaces
Homo sapiens (human)
DOID:178
  • vascular disease
  • Aliases:
    • vascular tissue disease
Homo sapiens (human)
DOID:5264
  • epithelioid leiomyosarcoma
Homo sapiens (human)
DOID:0110107
  • atrial heart septal defect 2
  • Aliases:
    • ASD2
    • atrial septal defect 2
Homo sapiens (human)
DOID:14768
  • Saethre-Chotzen syndrome
Homo sapiens (human)
DOID:12580
  • Cri-Du-Chat syndrome
  • Aliases:
    • 5p deletion syndrome
    • 5p partial monosomy syndrome
    • chromosome 5 short arm deletion syndrome
    • chromosome 5p deletion syndrome
Homo sapiens (human)
DOID:4330
  • non-Langerhans-cell histiocytosis
Homo sapiens (human)
DOID:9408
  • acute myocardial infarction
Homo sapiens (human)
DOID:9663
  • aphthous stomatitis
  • Aliases:
    • Aphtha
    • Aphthous ulceration
    • Canker sore
    • Oral aphthae
    • oral ulcer
Homo sapiens (human)
DOID:0110483
  • autosomal recessive nonsyndromic deafness 25
  • Aliases:
    • DFNB25
    • autosomal recessive deafness 25
Homo sapiens (human)
DOID:11719
  • oculopharyngeal muscular dystrophy
  • Aliases:
    • Muscular dystrophy, oculopharyngeal
Homo sapiens (human)
DOID:2712
  • phimosis
  • Aliases:
    • Tight foreskin
    • Tight frenulum
Homo sapiens (human)
DOID:0111238
  • congenital muscular dystrophy-dystroglycanopathy type A13
  • Aliases:
    • MDDGA13
    • Walker-Warburg syndrome or muscle-eye-brain disease, B3GNT1-related
    • Walker-Warburg syndrome or muscle-eye-brain disease, B4GNT1-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A13
Homo sapiens (human)
DOID:13580
  • cholestasis
  • Aliases:
    • Obstruction of bile duct
    • bile occlusion
Homo sapiens (human)
DOID:5204
  • fructose-1,6-bisphosphatase deficiency
  • Aliases:
    • fructose 1 phosphate aldolase deficiency
    • fructose-1,6-diphosphatase deficiency
Homo sapiens (human)
DOID:4531
  • mucoepidermoid carcinoma
  • Aliases:
    • MEC
Homo sapiens (human)

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Last updated: August 19, 2024