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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 7051 - 7075 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0110861
  • autosomal recessive polycystic kidney disease
  • Aliases:
    • Arpkd
    • Pkhd1
    • Polycystic Kidney Disease, Infantile, Type I
    • Polycystic Kidney and Hepatic Disease 1
Saccharomyces cerevisiae S288C
DOID:13166
  • allergic bronchopulmonary aspergillosis
  • Aliases:
    • pulmonary aspergillus disease
Homo sapiens (human)
DOID:0060681
  • autosomal dominant nocturnal frontal lobe epilepsy
  • Aliases:
    • ENFL
Homo sapiens (human)
DOID:0080322
  • polycystic kidney disease
Caenorhabditis elegans
DOID:824
  • periodontitis
  • Aliases:
    • chronic pericementitis
Xenopus laevis (African clawed frog)
DOID:0050697
  • chorioamnionitis
Rattus norvegicus (Norway rat)
DOID:0080226
  • autosomal dominant intellectual developmental disorder 56
  • Aliases:
    • autosomal dominant intellectual developmental disorder-56
    • autosomal dominant mental retardation 56
Homo sapiens (human)
DOID:2773
  • contact dermatitis
  • Aliases:
    • Contact dermatitis/eczema
    • Contact eczema
    • Dermatitis, venenata
    • dermatitis venenata
Homo sapiens (human)
DOID:0080071
  • mucolipidosis III alpha/beta
  • Aliases:
    • mucolipidosis III
    • pseudo-Hurler polydystrophy
Homo sapiens (human)
DOID:28
  • endocrine system disease
Xenopus tropicalis (tropical clawed frog)
DOID:0112171
  • wrinkly skin syndrome
  • Aliases:
    • WSS
Mus musculus (house mouse)
DOID:14261
  • fragile X syndrome
  • Aliases:
    • FRAGILE X MENTAL RETARDATION SYNDROME
    • MARKER X SYNDROME
    • MARTIN-BELL SYNDROME
Caenorhabditis elegans
DOID:0080845
  • omodysplasia 2
Caenorhabditis elegans
DOID:783
  • end stage renal disease
  • Aliases:
    • end stage renal failure
    • end-stage kidney disease
Saccharomyces cerevisiae S288C
DOID:1115
  • sarcoma
  • Aliases:
    • connective and soft tissue neoplasm
    • tumor of soft tissue and skeleton
Mus musculus (house mouse)
DOID:0111019
  • cone-rod dystrophy 12
  • Aliases:
    • CORD12
Drosophila melanogaster (fruit fly)
DOID:0070216
  • familial hyperinsulinemic hypoglycemia 3
  • Aliases:
    • HHF3
    • hyperinsulinemic hypoglycemia due to glucokinase deficiency
    • hyperinsulinism due to glucokinase deficiency
Drosophila melanogaster (fruit fly)
DOID:13374
  • fibrodysplasia ossificans progressiva
  • Aliases:
    • Stone Man Syndrome
    • myositis ossificans progressiva
    • progressive myositis ossificans
    • progressive ossifying myositis
Rattus norvegicus (Norway rat)
DOID:5813
  • purine nucleoside phosphorylase deficiency
  • Aliases:
    • PNP deficiency
    • Purine-Nucleoside Phosphorylase deficiency
    • deficiency of inosine phosphorylase
Mus musculus (house mouse)
DOID:0111403
  • mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations
  • Aliases:
    • MCCCHCM
Saccharomyces cerevisiae S288C
DOID:0080268
  • autosomal dominant nonsyndromic deafness 72
Homo sapiens (human)
DOID:0110501
  • autosomal recessive nonsyndromic deafness 44
  • Aliases:
    • DFNB44
    • autosomal recessive deafness 44
Mus musculus (house mouse)
DOID:9408
  • acute myocardial infarction
Rattus norvegicus (Norway rat)
DOID:0080294
  • Charcot-Marie-Tooth disease dominant intermediate G
Rattus norvegicus (Norway rat)
DOID:0050604
  • acrocapitofemoral dysplasia
Mus musculus (house mouse)
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

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