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 5076 - 5100 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:10541
  • microinvasive gastric cancer
  • Aliases:
    • Surface gastric cancer
    • early gastric cancer
Homo sapiens (human)
DOID:1826
  • epilepsy
  • Aliases:
    • epilepsy syndrome
    • epileptic syndrome
Homo sapiens (human)
DOID:0060695
  • hyperekplexia
  • Aliases:
    • Kok disease
    • congenital stiff man syndrome
    • familial startle disease
    • hereditary hyperekplexia
    • startle disease
Homo sapiens (human)
DOID:350
  • mastocytosis
  • Aliases:
    • mast cell hyperplasia
Homo sapiens (human)
DOID:0070468
  • Yoon-Bellen neurodevelopmental syndrome
  • Aliases:
    • YOBELN
Homo sapiens (human)
DOID:4606
  • bile duct cancer
  • Aliases:
    • Ca extrahepatic bile ducts
    • bile duct tumor
    • malignant neoplasm of the extrahepatic bile duct
Homo sapiens (human)
DOID:1907
  • malignant fibrous histiocytoma
  • Aliases:
    • Fibroxanthosarcoma
    • MFH
Homo sapiens (human)
DOID:13129
  • severe pre-eclampsia
  • Aliases:
    • Severe pre-eclampsia, with delivery
    • antepartum severe pre-eclampsia
    • postpartum severe pre-eclampsia
    • severe preeclampsia
Homo sapiens (human)
DOID:0060071
  • pre-malignant neoplasm
Homo sapiens (human)
DOID:0110533
  • autosomal recessive nonsyndromic deafness 88
  • Aliases:
    • DFNB88
    • autosomal recessive deafness 88
Homo sapiens (human)
DOID:0050800
  • cerebral creatine deficiency syndrome 1
  • Aliases:
    • CEREBRAL CREATINE DEFICIENCY SYNDROME 1
    • SLC6A8 deficiency
    • creatine transporter deficiency
Homo sapiens (human)
DOID:0110158
  • Charcot-Marie-Tooth disease type 2I
  • Aliases:
    • CMT2I
    • Charcot-Marie-Tooth neuropathy type 2I
Homo sapiens (human)
DOID:0060878
  • hypoparathyroidism-deafness-renal disease syndrome
  • Aliases:
    • Barakat syndrome
    • HDR syndrome
    • hypoparathyroidism, sensorineural deafness, and renal disease
Homo sapiens (human)
DOID:1561
  • cognitive disorder
  • Aliases:
    • cognitive disease
Homo sapiens (human)
DOID:4985
  • extraosseous Ewings sarcoma-primitive neuroepithelial tumor
  • Aliases:
    • extraosseous Ewing's tumor
    • extraosseous Ewing's tumour
    • extraosseous Ewings sarcoma-primitive neuroepithelial tumour
Homo sapiens (human)
DOID:13241
  • Behcet's disease
  • Aliases:
    • Adamantiades-Behcet disease
    • Behcet syndrome
    • Behet's syndrome
    • triple symptom complex
Homo sapiens (human)
DOID:0050463
  • campomelic dysplasia
  • Aliases:
    • Acampomelic Campomelic Dysplasia
Homo sapiens (human)
DOID:3901
  • vulvitis
Homo sapiens (human)
DOID:1679
  • cystitis
Homo sapiens (human)
DOID:3737
  • verrucous carcinoma
  • Aliases:
    • Warty carcinoma
    • verrucous squamous carcinoma
    • verrucous squamous cell carcinoma
Homo sapiens (human)
DOID:0050545
  • visceral heterotaxy
  • Aliases:
    • heterotaxia
    • situs ambiguus
Homo sapiens (human)
DOID:0111246
  • amyotrophic lateral sclerosis-parkinsonism/dementia complex 1
  • Aliases:
    • ALS-PDC
    • Amyotrophic lateral sclerosis-parkinsonism-dementia of Guam syndrome
    • Guam disease
    • Lytico-Bodig disease
    • PDALS
    • amyotrophic lateral sclerosis-parkinsonism/dementia complex of Guam
    • parkinsonism-dementia-ALS complex
Homo sapiens (human)
DOID:11165
  • common wart
Homo sapiens (human)
DOID:12835
  • quadriplegia
  • Aliases:
    • tetraplegia
Homo sapiens (human)
DOID:1475
  • lymphangioma
  • Aliases:
    • Congenital lymphangioma
    • benign lymphangioma
Homo sapiens (human)

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Last updated: August 19, 2024