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 14676 - 14700 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲ Source
DOID:0090044
  • dystonia 9
Saccharomyces cerevisiae S288C
DOID:0070376
  • developmental and epileptic encephalopathy 31B
  • Aliases:
    • DEE31B
Saccharomyces cerevisiae S288C
DOID:10609
  • rickets
  • Aliases:
    • active rickets
Saccharomyces cerevisiae S288C
DOID:0050625
  • biliary tract benign neoplasm
  • Aliases:
    • extrahepatic bile duct neoplasm
    • neoplasm of extrahepatic bile ducts
    • tumor of the extrahepatic bile duct
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:10286
  • prostate carcinoma
  • Aliases:
    • cancer of prostate
    • carcinoma of prostate
Saccharomyces cerevisiae S288C
DOID:0060108
  • brain glioma
  • Aliases:
    • lower grade glioma
Saccharomyces cerevisiae S288C
DOID:0111100
  • maturity-onset diabetes of the young type 2
  • Aliases:
    • MODY glucokinase-related
    • MODY type 2
    • MODY2
Saccharomyces cerevisiae S288C
DOID:0111237
  • congenital muscular dystrophy-dystroglycanopathy type A1
  • Aliases:
    • MDDGA1
    • Walker-Warburg syndrome or muscle-eye-brain disease, POMT1-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A1
Saccharomyces cerevisiae S288C
DOID:0050776
  • non-syndromic X-linked intellectual disability
  • Aliases:
    • non-specific X-linked mental retardation
Saccharomyces cerevisiae S288C
DOID:3753
  • Hermansky-Pudlak syndrome
Saccharomyces cerevisiae S288C
DOID:0110255
  • cataract 5 multiple types
  • Aliases:
    • CTRCT5
Saccharomyces cerevisiae S288C
DOID:5463
  • cochlear disease
Saccharomyces cerevisiae S288C
DOID:224
  • transient cerebral ischemia
  • Aliases:
    • TIA
    • TIA - Transient ischaemic attack
    • Transient cerebral ischaemia
    • Transient ischemic attacks
    • transient ischemic attack
Saccharomyces cerevisiae S288C
DOID:1059
  • intellectual disability
Saccharomyces cerevisiae S288C
DOID:684
  • hepatocellular carcinoma
  • Aliases:
    • Hepatoma
Saccharomyces cerevisiae S288C
DOID:3534
  • Lafora disease
  • Aliases:
    • Lafora Progressive Myoclonic Epilepsy
    • Lafora's disease
    • MYOCLONIC EPILEPSY OF LAFORA
Saccharomyces cerevisiae S288C
DOID:331
  • central nervous system disease
Saccharomyces cerevisiae S288C
DOID:9669
  • senile cataract
Saccharomyces cerevisiae S288C
DOID:0080465
  • developmental and epileptic encephalopathy 30
  • Aliases:
    • DEE30
    • early infantile epileptic encephalopathy 30
Saccharomyces cerevisiae S288C
DOID:10140
  • dry eye syndrome
  • Aliases:
    • Tear film insufficiency
    • dry eye disease
Saccharomyces cerevisiae S288C
DOID:4500
  • hypokalemia
  • Aliases:
    • hypopotassemia
    • potassium deficiency disorder
Saccharomyces cerevisiae S288C
DOID:0060308
  • autosomal recessive intellectual developmental disorder
  • Aliases:
    • autosomal recessive mental retardation
    • autosomal recessive non-syndromic mental retardation
Saccharomyces cerevisiae S288C
DOID:0050644
  • arterial calcification of infancy
  • Aliases:
    • generalized arterial calcification of infancy
    • idiopathic infantile arterial calcification
    • infantile arteriosclerosis
Saccharomyces cerevisiae S288C
DOID:0080566
  • congenital disorder of glycosylation In
  • Aliases:
    • congenital disorder of glycosylation 1n
Saccharomyces cerevisiae S288C

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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