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 1651 - 1675 of 7942 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:12165
  • retinal lattice degeneration
  • Aliases:
    • Palisade degeneration of retina
Homo sapiens (human)
DOID:0060746
  • basal laminar drusen
  • Aliases:
    • cuticular drusen
    • drusen of bruch membrane
    • early adult-onset grouped drusen
Homo sapiens (human)
DOID:0110860
  • polycystic kidney disease 3
  • Aliases:
    • Apkd3
    • Pkd3
    • Polycystic Kidney Disease, Adult, Type III
Saccharomyces cerevisiae S288C
DOID:9408
  • acute myocardial infarction
Saccharomyces cerevisiae S288C
DOID:0050665
  • fetal alcohol syndrome
Saccharomyces cerevisiae S288C
DOID:0080377
  • peroxisomal biogenesis disorder
Saccharomyces cerevisiae S288C
DOID:4001
  • ovarian carcinoma
Saccharomyces cerevisiae S288C
DOID:2377
  • multiple sclerosis
  • Aliases:
    • Generalized multiple sclerosis
    • insular sclerosis
Saccharomyces cerevisiae S288C
DOID:10976
  • membranous glomerulonephritis
  • Aliases:
    • membranous nephropathy
Saccharomyces cerevisiae S288C
DOID:8577
  • ulcerative colitis
  • Aliases:
    • Left-sided ulcerative colitis
Saccharomyces cerevisiae S288C
DOID:0080566
  • congenital disorder of glycosylation In
  • Aliases:
    • congenital disorder of glycosylation 1n
Saccharomyces cerevisiae S288C
DOID:0050332
  • enlarged vestibular aqueduct
Homo sapiens (human)
DOID:653
  • purine-pyrimidine metabolic disorder
  • Aliases:
    • inborn errors of purine-pyrimidine metabolism
Caenorhabditis elegans
DOID:0050833
  • orotic aciduria
Caenorhabditis elegans
DOID:0060363
  • glycerol kinase deficiency
Caenorhabditis elegans
DOID:13810
  • familial hypercholesterolemia
  • Aliases:
    • Fredrickson type IIa hyperlipoproteinemia
    • Fredrickson type IIa lipidaemia
    • familial hyperbetalipoproteinaemia
    • familial hypercholesteremia
    • hyperbetalipoproteinemia
    • type II hyperlipidemia
Caenorhabditis elegans
DOID:0090023
  • split hand-foot malformation 4
  • Aliases:
    • SHFM4
Homo sapiens (human)
DOID:0090027
  • split hand-foot malformation 2
  • Aliases:
    • SHFM2
Homo sapiens (human)
DOID:0090025
  • split hand-foot malformation 3
  • Aliases:
    • SHFM3
    • chromosome 10q24 duplication syndrome
    • distal limb deficiencies with micrognathia
Homo sapiens (human)
DOID:0090026
  • split hand-foot malformation 6
  • Aliases:
    • SHFM6
Homo sapiens (human)
DOID:0090022
  • split hand-foot malformation 5
  • Aliases:
    • SHFM5
Homo sapiens (human)
DOID:0090020
  • split hand-foot malformation
  • Aliases:
    • lobster-claw deformity
    • split-hand deformity
Homo sapiens (human)
DOID:2746
  • glycogen storage disease V
  • Aliases:
    • Glycogen storage disease 5
    • Glycogen storage disease, type V
    • McArdle's disease
    • glycogen storage disease type V
    • myophosphorylase deficiency
Mus musculus (house mouse)
DOID:2754
  • glycogen storage disease VI
  • Aliases:
    • Glycogen storage disease 6
    • Hers' disease
    • glycogen storage disease type VI
    • hepatic glycogen phosphorylase deficiency
    • hepatophosphorylase deficiency glycogenosis
Rattus norvegicus (Norway rat)
DOID:2754
  • glycogen storage disease VI
  • Aliases:
    • Glycogen storage disease 6
    • Hers' disease
    • glycogen storage disease type VI
    • hepatic glycogen phosphorylase deficiency
    • hepatophosphorylase deficiency glycogenosis
Mus musculus (house mouse)

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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