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 1176 - 1200 of 4621 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism
DOID:3571
  • liver cancer
  • Aliases:
    • Ca liver - primary
    • Resectable malignant neoplasm of Liver
    • hepatic cancer
    • hepatic neoplasm
    • malignant hepato-biliary neoplasm
    • malignant neoplasm of liver
    • malignant neoplasm of liver, not specified as primary or secondary
    • malignant neoplasm of liver, primary
    • malignant tumor of liver
    • neoplasm of liver
    • non-resectable primary hepatic malignant neoplasm
    • primary liver cancer
    • primary malignant neoplasm of liver
    • resectable malignant neoplasm of the liver
Homo sapiens (human)
DOID:3565
  • meningioma
  • Aliases:
    • meningeal neoplasm
    • meningothelial cell tumor
    • neoplasm of the meninges
    • primary Meningeal tumor
Homo sapiens (human)
DOID:3559
  • pseudomyxoma peritonei
  • Aliases:
    • mucinous Ascites
Homo sapiens (human)
DOID:3557
  • superior mesenteric artery syndrome
  • Aliases:
    • Wilkie's syndrome
Homo sapiens (human)
DOID:355
  • mast-cell sarcoma
Homo sapiens (human)
DOID:3540
  • choroid plexus cancer
  • Aliases:
    • tumor of choroid plexus
    • tumor of the Choroid Plexus
Homo sapiens (human)
DOID:3535
  • Unverricht-Lundborg syndrome
  • Aliases:
    • Unverricht - Lundborg disease
    • Unverricht's disease
    • Unverricht-Lundborg disease
Homo sapiens (human)
DOID:3534
  • Lafora disease
  • Aliases:
    • Lafora Progressive Myoclonic Epilepsy
    • Lafora's disease
    • MYOCLONIC EPILEPSY OF LAFORA
Homo sapiens (human)
DOID:3530
  • chronic wasting disease
Homo sapiens (human)
DOID:3529
  • congenital myopathy 1A
  • Aliases:
    • central core disease
    • central core myopathy
Homo sapiens (human)
DOID:3526
  • cerebral infarction
  • Aliases:
    • CVA - Cerebral infarction
    • Cerebral infarct
Homo sapiens (human)
DOID:3525
  • middle cerebral artery infarction
Homo sapiens (human)
DOID:3523
  • brain stem infarction
  • Aliases:
    • Brainstem infarction
Homo sapiens (human)
DOID:3516
  • adult fibrosarcoma
Homo sapiens (human)
DOID:3512
  • neurofibrosarcoma
  • Aliases:
    • Neurosarcoma
Homo sapiens (human)
DOID:3507
  • dermatofibrosarcoma protuberans
Homo sapiens (human)
DOID:3502
  • ampulla of Vater adenocarcinoma
  • Aliases:
    • ampullary adenocarcinoma
Homo sapiens (human)
DOID:3500
  • gallbladder adenocarcinoma
  • Aliases:
    • adenocarcinoma of the gallbladder
Homo sapiens (human)
DOID:350
  • mastocytosis
  • Aliases:
    • mast cell hyperplasia
Homo sapiens (human)
DOID:3498
  • pancreatic ductal adenocarcinoma
  • Aliases:
    • ductal adenocarcinoma of the pancreas
Homo sapiens (human)
DOID:3493
  • signet ring cell adenocarcinoma
  • Aliases:
    • Signet ring carcinoma
    • Signet ring cell carcinoma
Homo sapiens (human)
DOID:3492
  • mixed connective tissue disease
  • Aliases:
    • Connective tissue disease overlap syndrome
    • mixed collagen vascular disease
Homo sapiens (human)
DOID:3491
  • Turner syndrome
  • Aliases:
    • Bonnevie-Ullrich syndrome
    • Gonadal dysgenesis - Turner
    • Karyotype 45, X
    • Monosomy X
    • XO syndrome
    • monosomy X syndrome
Homo sapiens (human)
DOID:3490
  • Noonan syndrome
  • Aliases:
    • Turner's phenotype, karyotype normal
Homo sapiens (human)
DOID:349
  • systemic mastocytosis
  • Aliases:
    • SMCD - systemic mast cell disease
    • systemic tissue mast cell disease
Homo sapiens (human)

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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: August 19, 2024