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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 14251 - 14275 of 15957 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism Source
DOID:1391
  • Norum disease
  • Aliases:
    • LECITHIN CHOLESTEROL ACYLTRANSFERASE DEFICIENCY
    • lecithin acyltransferase deficiency
Mus musculus (house mouse)
DOID:1391
  • Norum disease
  • Aliases:
    • LECITHIN CHOLESTEROL ACYLTRANSFERASE DEFICIENCY
    • lecithin acyltransferase deficiency
Caenorhabditis elegans
DOID:1391
  • Norum disease
  • Aliases:
    • LECITHIN CHOLESTEROL ACYLTRANSFERASE DEFICIENCY
    • lecithin acyltransferase deficiency
Rattus norvegicus (Norway rat)
DOID:1391
  • Norum disease
  • Aliases:
    • LECITHIN CHOLESTEROL ACYLTRANSFERASE DEFICIENCY
    • lecithin acyltransferase deficiency
Saccharomyces cerevisiae S288C
DOID:1391
  • Norum disease
  • Aliases:
    • LECITHIN CHOLESTEROL ACYLTRANSFERASE DEFICIENCY
    • lecithin acyltransferase deficiency
Homo sapiens (human)
DOID:0060844
  • Norrie disease
  • Aliases:
    • Episkopi blindness
    • Norrie-Warburg disease
    • atrophia bulborum hereditaria
Homo sapiens (human)
DOID:0060844
  • Norrie disease
  • Aliases:
    • Episkopi blindness
    • Norrie-Warburg disease
    • atrophia bulborum hereditaria
Drosophila melanogaster (fruit fly)
DOID:0060844
  • Norrie disease
  • Aliases:
    • Episkopi blindness
    • Norrie-Warburg disease
    • atrophia bulborum hereditaria
Mus musculus (house mouse)
DOID:0060844
  • Norrie disease
  • Aliases:
    • Episkopi blindness
    • Norrie-Warburg disease
    • atrophia bulborum hereditaria
Rattus norvegicus (Norway rat)
DOID:0060902
  • Norman-Roberts syndrome
  • Aliases:
    • lissencephaly 2
    • lissencephaly syndrome, Norman-Roberts type
Rattus norvegicus (Norway rat)
DOID:0060902
  • Norman-Roberts syndrome
  • Aliases:
    • lissencephaly 2
    • lissencephaly syndrome, Norman-Roberts type
Mus musculus (house mouse)
DOID:0060902
  • Norman-Roberts syndrome
  • Aliases:
    • lissencephaly 2
    • lissencephaly syndrome, Norman-Roberts type
Homo sapiens (human)
DOID:0080691
  • Noonan syndrome-like disorder with loose anagen hair
Homo sapiens (human)
DOID:0080693
  • Noonan syndrome-like disorder with loose anagen hair 2
Rattus norvegicus (Norway rat)
DOID:0080693
  • Noonan syndrome-like disorder with loose anagen hair 2
Homo sapiens (human)
DOID:0080693
  • Noonan syndrome-like disorder with loose anagen hair 2
Mus musculus (house mouse)
DOID:0080693
  • Noonan syndrome-like disorder with loose anagen hair 2
Saccharomyces cerevisiae S288C
DOID:0080693
  • Noonan syndrome-like disorder with loose anagen hair 2
Xenopus laevis (African clawed frog)
DOID:0080693
  • Noonan syndrome-like disorder with loose anagen hair 2
Xenopus tropicalis (tropical clawed frog)
DOID:0080692
  • Noonan syndrome-like disorder with loose anagen hair 1
Homo sapiens (human)
DOID:3490
  • Noonan syndrome
  • Aliases:
    • Turner's phenotype, karyotype normal
Mus musculus (house mouse)
DOID:3490
  • Noonan syndrome
  • Aliases:
    • Turner's phenotype, karyotype normal
Rattus norvegicus (Norway rat)
DOID:3490
  • Noonan syndrome
  • Aliases:
    • Turner's phenotype, karyotype normal
Drosophila melanogaster (fruit fly)
DOID:3490
  • Noonan syndrome
  • Aliases:
    • Turner's phenotype, karyotype normal
Caenorhabditis elegans
DOID:3490
  • Noonan syndrome
  • Aliases:
    • Turner's phenotype, karyotype normal
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: December 9, 2024