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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 8001 - 8025 of 15957 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism Source
DOID:2216
  • factor V deficiency
  • Aliases:
    • Hereditary hypoproaccelerinaemia
    • Labile factor deficiency
    • Proaccelerin deficiency
    • deficiency, labile
Mus musculus (house mouse)
DOID:2215
  • factor VII deficiency
  • Aliases:
    • deficiency, stable
Mus musculus (house mouse)
DOID:2215
  • factor VII deficiency
  • Aliases:
    • deficiency, stable
Homo sapiens (human)
DOID:2215
  • factor VII deficiency
  • Aliases:
    • deficiency, stable
Rattus norvegicus (Norway rat)
DOID:12134
  • factor VIII deficiency
  • Aliases:
    • Congenital factor VIII disorder
    • Hemophilia A
    • Subhemophilia
    • classic hemophilia A
Mus musculus (house mouse)
DOID:12134
  • factor VIII deficiency
  • Aliases:
    • Congenital factor VIII disorder
    • Hemophilia A
    • Subhemophilia
    • classic hemophilia A
Homo sapiens (human)
DOID:12134
  • factor VIII deficiency
  • Aliases:
    • Congenital factor VIII disorder
    • Hemophilia A
    • Subhemophilia
    • classic hemophilia A
Rattus norvegicus (Norway rat)
DOID:12134
  • factor VIII deficiency
  • Aliases:
    • Congenital factor VIII disorder
    • Hemophilia A
    • Subhemophilia
    • classic hemophilia A
Xenopus laevis (African clawed frog)
DOID:2222
  • factor X deficiency
  • Aliases:
    • disease, Stuart-Prower
Mus musculus (house mouse)
DOID:2222
  • factor X deficiency
  • Aliases:
    • disease, Stuart-Prower
Rattus norvegicus (Norway rat)
DOID:2222
  • factor X deficiency
  • Aliases:
    • disease, Stuart-Prower
Homo sapiens (human)
DOID:2229
  • factor XI deficiency
  • Aliases:
    • Congenital factor XI deficiency
    • Hereditary factor XI deficiency disease
    • Rosenthal's disease
    • hemophilia C
    • plasma thromboplastin antecedent deficiency
Mus musculus (house mouse)
DOID:2229
  • factor XI deficiency
  • Aliases:
    • Congenital factor XI deficiency
    • Hereditary factor XI deficiency disease
    • Rosenthal's disease
    • hemophilia C
    • plasma thromboplastin antecedent deficiency
Homo sapiens (human)
DOID:2231
  • factor XII deficiency
  • Aliases:
    • Factor XII deficiency disease
    • Hageman Factor deficiency
    • deficiency, Hageman
Homo sapiens (human)
DOID:2231
  • factor XII deficiency
  • Aliases:
    • Factor XII deficiency disease
    • Hageman Factor deficiency
    • deficiency, Hageman
Mus musculus (house mouse)
DOID:2231
  • factor XII deficiency
  • Aliases:
    • Factor XII deficiency disease
    • Hageman Factor deficiency
    • deficiency, Hageman
Rattus norvegicus (Norway rat)
DOID:2211
  • factor XIII deficiency
  • Aliases:
    • Factor XIII deficiency disease
    • Hereditary factor XIII deficiency disease
    • deficiency, Laki-Lorand factor
Mus musculus (house mouse)
DOID:2211
  • factor XIII deficiency
  • Aliases:
    • Factor XIII deficiency disease
    • Hereditary factor XIII deficiency disease
    • deficiency, Laki-Lorand factor
Homo sapiens (human)
DOID:2211
  • factor XIII deficiency
  • Aliases:
    • Factor XIII deficiency disease
    • Hereditary factor XIII deficiency disease
    • deficiency, Laki-Lorand factor
Rattus norvegicus (Norway rat)
DOID:1962
  • fallopian tube disease
Rattus norvegicus (Norway rat)
DOID:1962
  • fallopian tube disease
Homo sapiens (human)
DOID:1962
  • fallopian tube disease
Mus musculus (house mouse)
DOID:0080944
  • familial Behcet-like autoinflammatory syndrome
  • Aliases:
    • A20 haploinsufficiency
Mus musculus (house mouse)
DOID:0080944
  • familial Behcet-like autoinflammatory syndrome
  • Aliases:
    • A20 haploinsufficiency
Homo sapiens (human)
DOID:0111420
  • familial GPIHBP1 deficiency
  • Aliases:
    • familial glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 deficiency
    • hyperlipoproteinemia type 1D
    • hyperlipoproteinemia type ID
Mus musculus (house mouse)
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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