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 1476 - 1500 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:3069
  • malignant astrocytoma
  • Aliases:
    • Astrocytic tumor
    • astrocytoma of Cerebrum
    • astrocytoma of brain
    • astroglioma
    • cerebral astrocytoma
Mus musculus (house mouse)
DOID:0060284
  • paroxysmal nocturnal hemoglobinuria
Mus musculus (house mouse)
DOID:4989
  • pancreatitis
Mus musculus (house mouse)
DOID:631
  • fibromyalgia
Mus musculus (house mouse)
DOID:252
  • alcoholic psychosis
  • Aliases:
    • Alcoholic psychoses
Mus musculus (house mouse)
DOID:1793
  • pancreatic cancer
  • Aliases:
    • Ca body of pancreas
    • Ca head of pancreas
    • Ca tail of pancreas
    • malignant neoplasm of body of pancreas
    • malignant neoplasm of head of pancreas
    • malignant neoplasm of tail of pancreas
    • pancreas neoplasm
    • pancreatic neoplasm
    • pancreatic tumor
Mus musculus (house mouse)
DOID:10241
  • thalassemia
  • Aliases:
    • Sickle-cell thalassemia with crisis
    • Sickle-cell thalassemia without crisis
    • thalassemia Hb-S disease with crisis
    • thalassemia Hb-S disease without crisis
Mus musculus (house mouse)
DOID:0110669
  • congenital myasthenic syndrome 14
  • Aliases:
    • CMS14
    • CMSTA3
    • congenital myasthenic syndrome 14, with tubular aggregates
    • congenital myasthenic syndrome with tubular aggregates 3
Mus musculus (house mouse)
DOID:0111459
  • classic galactosemia
  • Aliases:
    • GALT deficiency
    • galactose-1-phosphate uridyltransferase deficiency
    • galactosemia type 1
Mus musculus (house mouse)
DOID:0050731
  • vitamin B12 deficiency
  • Aliases:
    • cobalamin deficiency
    • hypocobalaminemia
Mus musculus (house mouse)
DOID:0050809
  • mucopolysaccharidosis IX
Mus musculus (house mouse)
DOID:11506
  • suppurative otitis media
  • Aliases:
    • Otitis media with effusion - purulent
    • Purulent otitis media
Mus musculus (house mouse)
DOID:0110798
  • hereditary spastic paraplegia 46
  • Aliases:
    • SPG46
    • autosomal recessive spastic paraplegia 46
    • autosomal recessive spastic paraplegia type 46
Mus musculus (house mouse)
DOID:10941
  • intracranial aneurysm
  • Aliases:
    • brain aneurysm
Mus musculus (house mouse)
DOID:1749
  • squamous cell carcinoma
  • Aliases:
    • epidermoid carcinoma
    • malignant squamous cell tumor
    • squamous carcinoma
    • squamous cell Epithelioma
    • squamous cell cancer
Mus musculus (house mouse)
DOID:3594
  • choriocarcinoma
  • Aliases:
    • Chorioepithelioma
Mus musculus (house mouse)
DOID:1024
  • leprosy
Mus musculus (house mouse)
DOID:399
  • tuberculosis
Mus musculus (house mouse)
DOID:0060319
  • cardiac arrest
  • Aliases:
    • cardiopulmonary arrest
    • circulatory arrest
Mus musculus (house mouse)
DOID:10933
  • obsessive-compulsive disorder
  • Aliases:
    • Anancastic neurosis
    • obsessive compulsive disorder
Mus musculus (house mouse)
DOID:0110777
  • hereditary spastic paraplegia 26
  • Aliases:
    • GM2 synthase deficiency
    • SPG26
    • autosomal recessive spastic paraplegia 26
    • autosomal recessive spastic paraplegia type 26
Mus musculus (house mouse)
DOID:5419
  • schizophrenia
  • Aliases:
    • schizophrenia-1
Mus musculus (house mouse)
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
Mus musculus (house mouse)
DOID:0110196
  • Charcot-Marie-Tooth disease type 4G
  • Aliases:
    • CMT4G
    • Charcot-Marie-Tooth neuropathy type 4G
    • HMSNR
    • autosomal recessive Charcot-Marie-Tooth disease type 4G
    • hereditary motor and sensory neuropathy Russe type
Mus musculus (house mouse)
DOID:9351
  • diabetes mellitus
  • Aliases:
    • diabetes
Mus musculus (house mouse)

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024