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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 6901 - 6925 of 15957 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism Source
DOID:0111027
  • hemochromatosis type 2A
  • Aliases:
    • HFE2A
Caenorhabditis elegans
DOID:0111027
  • hemochromatosis type 2A
  • Aliases:
    • HFE2A
Mus musculus (house mouse)
DOID:0111028
  • hemochromatosis type 4
  • Aliases:
    • HFE4
    • autosomal dominant hereditary hemochromatosis
    • ferroportin disease
    • hemochromatosis due to defect in ferroportin
Homo sapiens (human)
DOID:0111028
  • hemochromatosis type 4
  • Aliases:
    • HFE4
    • autosomal dominant hereditary hemochromatosis
    • ferroportin disease
    • hemochromatosis due to defect in ferroportin
Mus musculus (house mouse)
DOID:0111029
  • hemochromatosis type 1
  • Aliases:
    • HFE1
    • symptomatic form of HFE-related hereditary hemochromatosis
    • symptomatic form of classic hemochromatosis
    • symptomatic form of hemochromatosis type 1
Homo sapiens (human)
DOID:0111029
  • hemochromatosis type 1
  • Aliases:
    • HFE1
    • symptomatic form of HFE-related hereditary hemochromatosis
    • symptomatic form of classic hemochromatosis
    • symptomatic form of hemochromatosis type 1
Drosophila melanogaster (fruit fly)
DOID:0111029
  • hemochromatosis type 1
  • Aliases:
    • HFE1
    • symptomatic form of HFE-related hereditary hemochromatosis
    • symptomatic form of classic hemochromatosis
    • symptomatic form of hemochromatosis type 1
Xenopus laevis (African clawed frog)
DOID:0111029
  • hemochromatosis type 1
  • Aliases:
    • HFE1
    • symptomatic form of HFE-related hereditary hemochromatosis
    • symptomatic form of classic hemochromatosis
    • symptomatic form of hemochromatosis type 1
Mus musculus (house mouse)
DOID:0111029
  • hemochromatosis type 1
  • Aliases:
    • HFE1
    • symptomatic form of HFE-related hereditary hemochromatosis
    • symptomatic form of classic hemochromatosis
    • symptomatic form of hemochromatosis type 1
Caenorhabditis elegans
DOID:0111029
  • hemochromatosis type 1
  • Aliases:
    • HFE1
    • symptomatic form of HFE-related hereditary hemochromatosis
    • symptomatic form of classic hemochromatosis
    • symptomatic form of hemochromatosis type 1
Rattus norvegicus (Norway rat)
DOID:0111030
  • hemochromatosis type 3
  • Aliases:
    • HFE3
    • TFR2-related hemochromatosis
    • hemochromatosis due to defect in transferrin receptor 2
Mus musculus (house mouse)
DOID:0111030
  • hemochromatosis type 3
  • Aliases:
    • HFE3
    • TFR2-related hemochromatosis
    • hemochromatosis due to defect in transferrin receptor 2
Rattus norvegicus (Norway rat)
DOID:0111030
  • hemochromatosis type 3
  • Aliases:
    • HFE3
    • TFR2-related hemochromatosis
    • hemochromatosis due to defect in transferrin receptor 2
Saccharomyces cerevisiae S288C
DOID:0111030
  • hemochromatosis type 3
  • Aliases:
    • HFE3
    • TFR2-related hemochromatosis
    • hemochromatosis due to defect in transferrin receptor 2
Homo sapiens (human)
DOID:0111031
  • hemochromatosis type 5
  • Aliases:
    • FTH1-associated iron overload
    • FTH1-related iron overload
    • HFE5
Mus musculus (house mouse)
DOID:0111031
  • hemochromatosis type 5
  • Aliases:
    • FTH1-associated iron overload
    • FTH1-related iron overload
    • HFE5
Homo sapiens (human)
DOID:0111035
  • CADASIL 1
  • Aliases:
    • autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1
Drosophila melanogaster (fruit fly)
DOID:0111035
  • CADASIL 1
  • Aliases:
    • autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1
Homo sapiens (human)
DOID:0111035
  • CADASIL 1
  • Aliases:
    • autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1
Rattus norvegicus (Norway rat)
DOID:0111035
  • CADASIL 1
  • Aliases:
    • autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1
Caenorhabditis elegans
DOID:0111035
  • CADASIL 1
  • Aliases:
    • autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1
Mus musculus (house mouse)
DOID:0111037
  • glycine N-methyltransferase deficiency
  • Aliases:
    • GNMT deficiency
    • hypermethioninemia due to GNMT deficiency
    • hypermethioninemia due to glycine N-methyltransferase deficiency
Homo sapiens (human)
DOID:0111037
  • glycine N-methyltransferase deficiency
  • Aliases:
    • GNMT deficiency
    • hypermethioninemia due to GNMT deficiency
    • hypermethioninemia due to glycine N-methyltransferase deficiency
Mus musculus (house mouse)
DOID:0111037
  • glycine N-methyltransferase deficiency
  • Aliases:
    • GNMT deficiency
    • hypermethioninemia due to GNMT deficiency
    • hypermethioninemia due to glycine N-methyltransferase deficiency
Rattus norvegicus (Norway rat)
DOID:0111039
  • hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase
  • Aliases:
    • hypermethioninemia due to S-adenosylhomocysteine hydrolase deficiency
    • psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency
Homo sapiens (human)
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Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024