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 10751 - 10775 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:4440
  • seminoma
  • Aliases:
    • Seminoma, Pure
Caenorhabditis elegans
DOID:8440
  • ileus
  • Aliases:
    • Ileus of intestine
Caenorhabditis elegans
DOID:3042
  • allergic contact dermatitis
Caenorhabditis elegans
DOID:2316
  • brain ischemia
  • Aliases:
    • Ischaemic encephalopathy
    • Ischemic encephalopathy
    • cerebral ischemia
Caenorhabditis elegans
DOID:289
  • endometriosis
Caenorhabditis elegans
DOID:8725
  • vascular dementia
  • Aliases:
    • Multi Infarct Dementia
    • multifocal dementia
Caenorhabditis elegans
DOID:332
  • amyotrophic lateral sclerosis
  • Aliases:
    • ALS
    • Lou Gehrig's disease
    • motor neuron disease, bulbar
Caenorhabditis elegans
DOID:9253
  • gastrointestinal stromal tumor
  • Aliases:
    • GANT
    • GIST
    • Stromal tumor of gastrointestinal tract
    • Stromal tumour of gastrointestinal tract
    • gastrointestinal stromal tumour
Caenorhabditis elegans
DOID:0090005
  • Schwartz-Jampel syndrome 1
  • Aliases:
    • Aberfeld syndrome
    • Burton skeletal dysplasia
    • Burton syndrome
    • Catel-Hempel syndrome
    • Catel-Hempel type dysostosis enchondralis metaepiphysaria
    • Schwartz-Jampel syndrome type 1
    • Schwartz-Jampel-Aberfeld syndrome
    • myotonic chondrodystrophy
    • myotonic myopathy, dwarfism, chondrodystrophy, ocular and facial anomalies
    • osteochondromuscular dystrophy
Caenorhabditis elegans
DOID:13481
  • thanatophoric dysplasia
Caenorhabditis elegans
DOID:0090032
  • Silverman-Handmaker type dyssegmental dysplasia
Caenorhabditis elegans
DOID:0060770
  • dextro-looped transposition of the great arteries
  • Aliases:
    • D-TGA
    • DTGA1
    • congenitally uncorrected transposition of the great arteries
    • congenitally uncorrected transposition of the great vessels
    • isolated ventriculoarterial discordance
    • ventriculoarterial discordance with atrioventricular concordance
Caenorhabditis elegans
DOID:3407
  • carotid artery disease
  • Aliases:
    • disorder of carotid artery
Caenorhabditis elegans
DOID:9266
  • cystinuria
Caenorhabditis elegans
DOID:8645
  • subacute delirium
Caenorhabditis elegans
DOID:437
  • myasthenia gravis
Caenorhabditis elegans
DOID:1849
  • cannabis dependence
Caenorhabditis elegans
DOID:9974
  • drug dependence
Caenorhabditis elegans
DOID:2377
  • multiple sclerosis
  • Aliases:
    • Generalized multiple sclerosis
    • insular sclerosis
Caenorhabditis elegans
DOID:0080556
  • congenital disorder of glycosylation Id
  • Aliases:
    • congenital disorder of glycosylation 1d
Caenorhabditis elegans
DOID:5212
  • congenital disorder of glycosylation
  • Aliases:
    • carbohydrate-deficient glycoprotein syndrome
Caenorhabditis elegans
DOID:0111394
  • mucopolysaccharidosis type IIIB
  • Aliases:
    • MPS3B
    • MPSIIIB
    • Mucopoly-saccharidosis type 3B
    • Mucopolysaccharidosis type 3B
    • N-acetyl-alpha-glucosaminidase deficiency
    • NAGLU deficiency
    • Sanfilippo syndrome type B
    • mucopolysaccharidosis type IIIB (Sanfilippo B)
Caenorhabditis elegans
DOID:12801
  • mucopolysaccharidosis III
  • Aliases:
    • Mucopolysaccharidosis, MPS-III
    • N-sulphoglucosamine sulphohydrolase deficiency
    • Sanfilippo's syndrome
    • heparan sulfate sulfatase deficiency
Caenorhabditis elegans
DOID:0110178
  • Charcot-Marie-Tooth disease axonal type 2V
  • Aliases:
    • CMT2V
    • Charcot-Marie-Tooth neuropathy type 2V
    • autosomal dominant Charcot-Marie-Tooth disease type 2V
    • autosomal dominant axonal Charcot-Marie-Tooth disease type 2V
Caenorhabditis elegans
DOID:10754
  • otitis media
Caenorhabditis elegans

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 9, 2024