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 2851 - 2875 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:8233
  • inflammatory liposarcoma
Homo sapiens (human)
DOID:12341
  • retroperitoneal sarcoma
Homo sapiens (human)
DOID:0110726
  • neuronal ceroid lipofuscinosis 2
  • Aliases:
    • CLN2
    • neuronal ceroid lipofuscinosis 2 variable age at onset
Homo sapiens (human)
DOID:162
  • cancer
  • Aliases:
    • malignant neoplasm
    • malignant tumor
    • primary cancer
Homo sapiens (human)
DOID:4030
  • eosinophilic gastritis
Homo sapiens (human)
DOID:0110732
  • neuronal ceroid lipofuscinosis 11
  • Aliases:
    • CLN11
Homo sapiens (human)
DOID:0060425
  • chromosome 8q21.11 deletion syndrome
  • Aliases:
    • 8q21.11 microdeletion syndrome
Homo sapiens (human)
DOID:3209
  • junctional epidermolysis bullosa
  • Aliases:
    • congenital junctional epidermolysis bullosa
Homo sapiens (human)
DOID:9505
  • cannabis abuse
  • Aliases:
    • marijuana abuse
Homo sapiens (human)
DOID:0110249
  • cataract 11 multiple types
  • Aliases:
    • CTRCT11
Homo sapiens (human)
DOID:13207
  • proliferative diabetic retinopathy
  • Aliases:
    • PDR
Homo sapiens (human)
DOID:0080197
  • congenital muscular dystrophy with cataracts and intellectual disability
Homo sapiens (human)
DOID:0080029
  • autosomal recessive spinocerebellar ataxia 16
  • Aliases:
    • SCAR16
Homo sapiens (human)
DOID:0050574
  • L-2-hydroxyglutaric aciduria
  • Aliases:
    • L-2-HYDROXYGLUTARIC ACIDEMIA
Homo sapiens (human)
DOID:0110567
  • autosomal dominant nonsyndromic deafness 41
  • Aliases:
    • DFNA41
    • autosomal dominant deafness 41
Homo sapiens (human)
DOID:4737
  • somatoform disorder
  • Aliases:
    • physiological malfunction arising from mental factor
    • psychophysiologic disorder
    • psychosomatic disorder
Homo sapiens (human)
DOID:3895
  • apocrine adenoma
  • Aliases:
    • tubular Apocrine adenoma
Homo sapiens (human)
DOID:12804
  • mucopolysaccharidosis IV
  • Aliases:
    • Mucopolysaccharidosis, MPS-IV
    • deficiency of N-acetylgalactosamine-6-sulphatase
    • deficiency of chondroitinsulphatase
    • galactosamine-6-sulfatase deficiency
Homo sapiens (human)
DOID:0111421
  • familial apolipoprotein A5 deficiency
  • Aliases:
    • familial APOA5 deficiency
    • familial apolipoprotein A-V deficiency
Homo sapiens (human)
DOID:0110246
  • cataract 26 multiple types
  • Aliases:
    • CTRCT26
Homo sapiens (human)
DOID:0090045
  • childhood onset GLUT1 deficiency syndrome 2
Homo sapiens (human)
DOID:1060
  • Hartnup disease
  • Aliases:
    • Neutral 1 amino acid transport defect
    • deficiency of tryptophan oxygenase
    • neutral amino acid transport defect
Homo sapiens (human)
DOID:1485
  • cystic fibrosis
  • Aliases:
    • CF
    • mucoviscidosis
Homo sapiens (human)
DOID:5614
  • eye disease
Homo sapiens (human)
DOID:11963
  • esophagitis
  • Aliases:
    • acute esophagitis
Homo sapiens (human)

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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: August 19, 2024