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 1151 - 1175 of 7942 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:0110429
  • dilated cardiomyopathy 1H
  • Aliases:
    • dilated cardiomyopathy with conduction defect
Rattus norvegicus (Norway rat)
DOID:0060643
  • primary sclerosing cholangitis
Rattus norvegicus (Norway rat)
DOID:13976
  • peptic esophagitis
  • Aliases:
    • Peptic reflux disease
    • Reflux oesophagitis
    • reflux esophagitis
Rattus norvegicus (Norway rat)
DOID:2352
  • hemochromatosis
  • Aliases:
    • Haemochromatosis
    • diabetes bronze
    • iron storage disorder
Rattus norvegicus (Norway rat)
DOID:289
  • endometriosis
Rattus norvegicus (Norway rat)
DOID:6364
  • migraine
  • Aliases:
    • migraine disorder
    • migraine variant
    • migraine with or without aura
Rattus norvegicus (Norway rat)
DOID:409
  • liver disease
  • Aliases:
    • disorder of liver
    • hepatic disorder
Rattus norvegicus (Norway rat)
DOID:1270
  • hereditary hemorrhagic telangiectasia
  • Aliases:
    • Osler hemorrhagic telangiectasia syndrome
    • Osler-Weber-Rendu disease
    • Rendu-Osler-Weber disease
Rattus norvegicus (Norway rat)
DOID:2043
  • hepatitis B
  • Aliases:
    • chronic hepatitis B
    • hepatitis B infection
Rattus norvegicus (Norway rat)
DOID:1227
  • neutropenia
Mus musculus (house mouse)
DOID:12800
  • mucopolysaccharidosis VI
  • Aliases:
    • MPS VI - Maroteaux-Lamy syndrome
    • Maroteaux - Lamy syndrome
    • Maroteaux-Lamy syndrome
    • arylsulfatase B deficiency
    • deficiency of N-acetylgalactosamine-4-sulfatase
Mus musculus (house mouse)
DOID:12849
  • autistic disorder
  • Aliases:
    • Kanner's syndrome
    • autism
    • autistic disorder of childhood onset
    • childhood autism
    • infantile autism
Mus musculus (house mouse)
DOID:13976
  • peptic esophagitis
  • Aliases:
    • Peptic reflux disease
    • Reflux oesophagitis
    • reflux esophagitis
Mus musculus (house mouse)
DOID:0050475
  • Weill-Marchesani syndrome
  • Aliases:
    • GEMSS syndrome
    • Marchesani-Weill Syndrome
    • Mesodermal Dysmorphodystrophy, Congenital
    • Spherophakia Brachymorphia Syndrome
    • congenital mesodermal dystrophy
Mus musculus (house mouse)
DOID:12895
  • keratoconjunctivitis sicca
  • Aliases:
    • KCS
Mus musculus (house mouse)
DOID:4398
  • pustulosis of palm and sole
  • Aliases:
    • Acropustulosis
    • Palmoplantar Pustulosis
    • Pustular psoriasis of the palms and/or soles
Mus musculus (house mouse)
DOID:0081120
  • Graves ophthalmopathy
  • Aliases:
    • Graves orbitopathy
    • Thyroid associated ophthalmopathy
    • thyroid eye disease
Mus musculus (house mouse)
DOID:3458
  • breast adenocarcinoma
  • Aliases:
    • Mammary adenocarcinoma
Mus musculus (house mouse)
DOID:10003
  • sensorineural hearing loss
  • Aliases:
    • High Frequency Hearing Loss
    • High frequency deafness
    • Perceptive deafness
    • Perceptive hearing loss
    • Perceptive hearing loss or deafness
    • Sensorineural Deafness
    • Sensory hearing loss
    • central hearing loss
    • high-frequency hearing loss
Mus musculus (house mouse)
DOID:4306
  • radiculopathy
  • Aliases:
    • pinched nerve
Mus musculus (house mouse)
DOID:0060643
  • primary sclerosing cholangitis
Mus musculus (house mouse)
DOID:1679
  • cystitis
Mus musculus (house mouse)
DOID:5463
  • cochlear disease
Mus musculus (house mouse)
DOID:614
  • lymphopenia
  • Aliases:
    • Lymphocytopenia
Mus musculus (house mouse)
DOID:8515
  • Cor pulmonale
  • Aliases:
    • cardiopulmonary disease
    • pulmonary heart disease
Mus musculus (house mouse)

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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


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Last updated: August 19, 2024