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 1426 - 1450 of 15957 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:0080555
  • congenital disorder of glycosylation Ic
  • Aliases:
    • congenital disorder of glycosylation 1c
Drosophila melanogaster (fruit fly)
DOID:0060496
  • respiratory allergy
  • Aliases:
    • airway allergy
Caenorhabditis elegans
DOID:0110705
  • hypotrichosis 8
  • Aliases:
    • Hypt8
    • Lah3
    • hypotrichosis, localized, autosomal recessive 3
Caenorhabditis elegans
DOID:0080071
  • mucolipidosis III alpha/beta
  • Aliases:
    • mucolipidosis III
    • pseudo-Hurler polydystrophy
Danio rerio (zebrafish)
DOID:0080070
  • mucolipidosis II alpha/beta
  • Aliases:
    • I-cell disease
    • inclusion-cell disease
    • mucolipidosis II
Danio rerio (zebrafish)
DOID:0080488
  • mucolipidosis
Danio rerio (zebrafish)
DOID:0070253
  • congenital disorder of glycosylation type IIa
  • Aliases:
    • Alkuraya syndrome
    • CDG IIa
    • CDG2A
    • CDGIIa
    • CDGS2
    • carbohydrate-deficient glycoprotein syndrome, type II
    • congenital disorder of glycosylation, type IIa
    • mental retardation, growth retardation, prominent columella, and open mouth
Caenorhabditis elegans
DOID:0110242
  • cataract 13 with adult i phenotype
  • Aliases:
    • CTRCT13
Caenorhabditis elegans
DOID:4752
  • multiple system atrophy
  • Aliases:
    • Shy-Drager syndrome
Caenorhabditis elegans
DOID:0070537
  • spastic tetraplegia, thin corpus callosum, and progressive microcephaly
  • Aliases:
    • SPATCCM
Caenorhabditis elegans
DOID:0050994
  • episodic ataxia type 6
Caenorhabditis elegans
DOID:13544
  • low tension glaucoma
  • Aliases:
    • Normal tension glaucoma
Caenorhabditis elegans
DOID:0070093
  • schizophrenia 18
  • Aliases:
    • Chromosome 7q36.3 Duplication Syndrome, 362-Kb
    • SCZD18
Caenorhabditis elegans
DOID:0060650
  • dicarboxylic aminoaciduria
  • Aliases:
    • glutamate-aspartate transport defect
Caenorhabditis elegans
DOID:0080442
  • developmental and epileptic encephalopathy 41
  • Aliases:
    • DEE41
    • early infantile epileptic encephalopathy 41
Caenorhabditis elegans
DOID:0060696
  • hyperekplexia 1
  • Aliases:
    • HKPX1
Danio rerio (zebrafish)
DOID:0060695
  • hyperekplexia
  • Aliases:
    • Kok disease
    • congenital stiff man syndrome
    • familial startle disease
    • hereditary hyperekplexia
    • startle disease
Danio rerio (zebrafish)
DOID:0081182
  • autosomal recessive intellectual developmental disorder 6
Caenorhabditis elegans
DOID:331
  • central nervous system disease
Caenorhabditis elegans
DOID:0060823
  • syndromic X-linked intellectual disability 94
  • Aliases:
    • MRX94
    • MRXS29
    • mental retardation, X-linked 94
    • syndromic X-linked intellectual disability due to GRIA3 anomalies
    • syndromic X-linked mental retardation 29
    • syndromic X-linked mental retardation Wu type
Caenorhabditis elegans
DOID:5418
  • schizoaffective disorder
Caenorhabditis elegans
DOID:0081235
  • autosomal recessive intellectual developmental disorder 76
Caenorhabditis elegans
DOID:0050523
  • adult T-cell leukemia/lymphoma
  • Aliases:
    • Adult T-cell leukemia/lymphoma (HTLV-1 positive)
    • adult T-cell leukemia
Caenorhabditis elegans
DOID:0111343
  • lateral meningocele syndrome
  • Aliases:
    • Lehman syndrome
Caenorhabditis elegans
DOID:9245
  • Alagille syndrome
  • Aliases:
    • Alagille-Watson syndrome
    • Arteriohepatic dysplasia
Caenorhabditis elegans

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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: December 9, 2024