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 2451 - 2475 of 7942 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:2231
  • factor XII deficiency
  • Aliases:
    • Factor XII deficiency disease
    • Hageman Factor deficiency
    • deficiency, Hageman
Homo sapiens (human)
DOID:0060362
  • punctate palmoplantar keratoderma type III
  • Aliases:
    • acrokeratoelastoidosis of Costa
    • punctate palmoplantar hyperkeratosis type 3
    • punctate palmoplantar keratoderma type 3
Homo sapiens (human)
DOID:0110970
  • brachydactyly type C
  • Aliases:
    • BDC
Homo sapiens (human)
DOID:0050581
  • brachydactyly
Homo sapiens (human)
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:4608
  • common bile duct neoplasm
  • Aliases:
    • neoplasm of common bile duct
Saccharomyces cerevisiae S288C
DOID:0080664
  • diaphyseal medullary stenosis with malignant fibrous histiocytoma
  • Aliases:
    • Hardcastle syndrome
    • bone dysplasia-medullary fibrosarcoma syndrome
    • diaphyseal medullary stenosis-malignant fibrous histiocytoma syndrome
Saccharomyces cerevisiae S288C
DOID:166
  • melanotic neuroectodermal tumor
  • Aliases:
    • Infantile Melanotic neuroectodermal neoplasm
    • Melanotic neuroectodermal tumor of infancy
    • Melanotic neuroectodermal tumour of infancy
    • Pigmented neuroectodermal tumour of infancy
    • melanotic neuroectodermal tumour
Homo sapiens (human)
DOID:5325
  • Roberts syndrome
  • Aliases:
    • LONG BONE DEFICIENCIES ASSOCIATED WITH CLEFT LIP-PALATE
    • RBS
    • Roberts-Sc Phocomelia Syndrome
    • SC phocomelia syndrome
Homo sapiens (human)
DOID:0050536
  • obsolete SC phocomelia syndrome
  • Aliases:
    • Hypomelia Hypotrichosis Facial hemangioma syndrome
    • SC PSEUDOTHALIDOMIDE SYNDROME
Homo sapiens (human)
DOID:0081419
  • childhood-onset dystonia with optic atrophy and basal ganglia abnormalities
  • Aliases:
    • DYSTONIA 29, CHILDHOOD-ONSET
    • DYTOABG
    • MECR-related neurologic disorder
    • MEPAN syndrome
    • Mitochondrial Enoyl CoA Reductase Protein-Associated Neurodegeneration
Homo sapiens (human)
DOID:0111756
  • Leber hereditary optic neuropathy with demyelinating disease of CNS
Homo sapiens (human)
DOID:0080433
  • developmental and epileptic encephalopathy 51
  • Aliases:
    • DEE51
    • early infantile epileptic encephalopathy 51
Homo sapiens (human)
DOID:0080433
  • developmental and epileptic encephalopathy 51
  • Aliases:
    • DEE51
    • early infantile epileptic encephalopathy 51
Saccharomyces cerevisiae S288C
DOID:2316
  • brain ischemia
  • Aliases:
    • Ischaemic encephalopathy
    • Ischemic encephalopathy
    • cerebral ischemia
Saccharomyces cerevisiae S288C
DOID:0112222
  • developmental and epileptic encephalopathy 88
  • Aliases:
    • DEE88
    • early infantile epileptic encephalopathy 88
Homo sapiens (human)
DOID:0081219
  • autosomal recessive intellectual developmental disorder 57
Homo sapiens (human)
DOID:0050689
  • brachydactyly-syndactyly syndrome
Homo sapiens (human)
DOID:0050117
  • disease by infectious agent
  • Aliases:
    • infectious disease
Homo sapiens (human)
DOID:10457
  • Legionnaires' disease
  • Aliases:
    • Infection by Legionella pneumophilia
    • Legionella
    • Legionella pneumonia
    • Legionnaire's disease
Homo sapiens (human)
DOID:14176
  • selective IgG deficiency disease
  • Aliases:
    • Immunoglobin G subclass deficiency
    • Selective IgG Immunodeficiency
    • Selective Immunoglobulin G Subclass deficiency
    • Selective deficiency of IgG
    • Selective immunoglobulin G deficiency
Homo sapiens (human)
DOID:9861
  • miliary tuberculosis
  • Aliases:
    • Disseminated tuberculosis
    • Tuberculosis miliaris disseminata
    • acute miliary tuberculosis
    • generalized tuberculosis
Homo sapiens (human)
DOID:14239
  • gastrointestinal tularemia
  • Aliases:
    • Enteric tularemia
    • intestinal tularaemia
Homo sapiens (human)
DOID:12375
  • bronchopneumonia
  • Aliases:
    • Chest infection - bronchopneumonia
    • bronchial pneumonia
    • lobular pneumonia
Homo sapiens (human)
DOID:0060496
  • respiratory allergy
  • Aliases:
    • airway allergy
Homo sapiens (human)

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