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 7501 - 7525 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:1712
  • aortic valve stenosis
  • Aliases:
    • Aortic stenosis
    • Rheumatic aortic stenosis
    • rheumatic aortic valve stenosis
Saccharomyces cerevisiae S288C
DOID:0050866
  • oral squamous cell carcinoma
  • Aliases:
    • mouth squamous cell carcinoma
Saccharomyces cerevisiae S288C
DOID:178
  • vascular disease
  • Aliases:
    • vascular tissue disease
Saccharomyces cerevisiae S288C
DOID:8778
  • Crohn's disease
  • Aliases:
    • Crohn disease
    • Crohn's disease of colon
    • Crohn's disease of large bowel
    • Granulomatous Colitis
    • Pediatric Crohn's disease
Saccharomyces cerevisiae S288C
DOID:0111458
  • galactose epimerase deficiency
  • Aliases:
    • GALE deficiency
    • GALE-D
    • UDP-galactose-4-epimerase deficiency
    • epimerase deficiency galactosemia
    • galactosemia III
    • galactosemia type 3
    • uridine diphosphate galactose-4-epimerase deficiency
Saccharomyces cerevisiae S288C
DOID:0080563
  • congenital disorder of glycosylation Ik
  • Aliases:
    • congenital disorder of glycosylation 1k
Saccharomyces cerevisiae S288C
DOID:0080199
  • colorectal carcinoma
Saccharomyces cerevisiae S288C
DOID:3068
  • glioblastoma
  • Aliases:
    • GBM
    • adult glioblastoma multiforme
    • glioblastoma multiforme
    • grade IV adult Astrocytic tumor
    • primary glioblastoma multiforme
    • spongioblastoma multiforme
Saccharomyces cerevisiae S288C
DOID:0110184
  • Charcot-Marie-Tooth disease type 4J
  • Aliases:
    • CMT4J
    • autosomal recessive Charcot-Marie-Tooth disease type 4J
Saccharomyces cerevisiae S288C
DOID:440
  • neuromuscular disease
Saccharomyces cerevisiae S288C
DOID:1588
  • thrombocytopenia
Saccharomyces cerevisiae S288C
DOID:1824
  • status epilepticus
  • Aliases:
    • Grand mal status
Saccharomyces cerevisiae S288C
DOID:1591
  • renovascular hypertension
Saccharomyces cerevisiae S288C
DOID:0110297
  • autosomal recessive limb-girdle muscular dystrophy type 2K
  • Aliases:
    • LGMD2K
    • MDDGC1
    • limb-girdle muscular dystrophy-intellectual disability syndrome
    • muscular dystrophy limb-girdle type 2K
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C 1
Saccharomyces cerevisiae S288C
DOID:5813
  • purine nucleoside phosphorylase deficiency
  • Aliases:
    • PNP deficiency
    • Purine-Nucleoside Phosphorylase deficiency
    • deficiency of inosine phosphorylase
Saccharomyces cerevisiae S288C
DOID:0080562
  • congenital disorder of glycosylation Ij
  • Aliases:
    • Congenital disorder of glycosylation 1j
Saccharomyces cerevisiae S288C
DOID:0081376
  • obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy
Saccharomyces cerevisiae S288C
DOID:13580
  • cholestasis
  • Aliases:
    • Obstruction of bile duct
    • bile occlusion
Saccharomyces cerevisiae S288C
DOID:331
  • central nervous system disease
Saccharomyces cerevisiae S288C
DOID:0111352
  • D-2-hydroxyglutaric aciduria 2
  • Aliases:
    • D2HGA2
Saccharomyces cerevisiae S288C
DOID:0111077
  • pyruvate kinase deficiency of red cells
  • Aliases:
    • PK deficiency
    • hemolytic anemia due to red cell pyruvate kinase deficiency
    • pyruvate kinase deficiency of erythrocyte
Saccharomyces cerevisiae S288C
DOID:9282
  • ocular hypertension
Saccharomyces cerevisiae S288C
DOID:1287
  • cardiovascular system disease
  • Aliases:
    • disease of subdivision of hemolymphoid system
Saccharomyces cerevisiae S288C
DOID:0080557
  • congenital disorder of glycosylation Ie
  • Aliases:
    • congenital disorder of glycosylation 1e
Saccharomyces cerevisiae S288C
DOID:0111240
  • congenital muscular dystrophy-dystroglycanopathy type A2
  • Aliases:
    • MDDGA2
    • Walker-Warburg syndrome or muscle-eye-brain disease, POMT2-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A2
Saccharomyces cerevisiae S288C

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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