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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 5876 - 5900 of 15957 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:0080940
  • hereditary angioedema type III
Mus musculus (house mouse)
DOID:2231
  • factor XII deficiency
  • Aliases:
    • Factor XII deficiency disease
    • Hageman Factor deficiency
    • deficiency, Hageman
Mus musculus (house mouse)
DOID:0111907
  • thrombophilia due to thrombin defect
  • Aliases:
    • THPH1
    • prothrombin-related thrombophilia
    • thrombophilia due to factor 2 defect
Homo sapiens (human)
DOID:2211
  • factor XIII deficiency
  • Aliases:
    • Factor XIII deficiency disease
    • Hereditary factor XIII deficiency disease
    • deficiency, Laki-Lorand factor
Homo sapiens (human)
DOID:9286
  • priapism
  • Aliases:
    • Mentulagra
Homo sapiens (human)
DOID:11247
  • disseminated intravascular coagulation
  • Aliases:
    • DIC
    • Defibrination syndrome
    • Diffuse or disseminated intravascular coagulation
Rattus norvegicus (Norway rat)
DOID:0080630
  • B-lymphoblastic leukemia/lymphoma
  • Aliases:
    • B lymphoblastic leukemia/lymphoma
    • B-ALL
    • precursor B lymphoblastic lymphoma/leukemia
Rattus norvegicus (Norway rat)
DOID:0111907
  • thrombophilia due to thrombin defect
  • Aliases:
    • THPH1
    • prothrombin-related thrombophilia
    • thrombophilia due to factor 2 defect
Rattus norvegicus (Norway rat)
DOID:2211
  • factor XIII deficiency
  • Aliases:
    • Factor XIII deficiency disease
    • Hereditary factor XIII deficiency disease
    • deficiency, Laki-Lorand factor
Rattus norvegicus (Norway rat)
DOID:9286
  • priapism
  • Aliases:
    • Mentulagra
Rattus norvegicus (Norway rat)
DOID:0111907
  • thrombophilia due to thrombin defect
  • Aliases:
    • THPH1
    • prothrombin-related thrombophilia
    • thrombophilia due to factor 2 defect
Mus musculus (house mouse)
DOID:2211
  • factor XIII deficiency
  • Aliases:
    • Factor XIII deficiency disease
    • Hereditary factor XIII deficiency disease
    • deficiency, Laki-Lorand factor
Mus musculus (house mouse)
DOID:9286
  • priapism
  • Aliases:
    • Mentulagra
Mus musculus (house mouse)
DOID:2235
  • prothrombin deficiency
  • Aliases:
    • Congenital factor II deficiency
    • Hereditary factor II deficiency disease
    • hypoprothrombinemia
Mus musculus (house mouse)
DOID:12259
  • hemophilia B
  • Aliases:
    • Congenital factor IX deficiency
    • Congenital factor IX disorder
    • deficiency, functional factor IX
    • factor IX deficiency
Mus musculus (house mouse)
DOID:8506
  • bullous pemphigoid
Mus musculus (house mouse)
DOID:11695
  • portal vein thrombosis
Mus musculus (house mouse)
DOID:8536
  • herpes zoster
  • Aliases:
    • Shingles
    • herpes zona
Mus musculus (house mouse)
DOID:8337
  • appendicitis
  • Aliases:
    • acute appendicitis
    • acute appendicitis with generalized peritonitis
    • acute appendicitis with peritoneal abscess
Mus musculus (house mouse)
DOID:2235
  • prothrombin deficiency
  • Aliases:
    • Congenital factor II deficiency
    • Hereditary factor II deficiency disease
    • hypoprothrombinemia
Homo sapiens (human)
DOID:12259
  • hemophilia B
  • Aliases:
    • Congenital factor IX deficiency
    • Congenital factor IX disorder
    • deficiency, functional factor IX
    • factor IX deficiency
Homo sapiens (human)
DOID:8506
  • bullous pemphigoid
Homo sapiens (human)
DOID:11695
  • portal vein thrombosis
Homo sapiens (human)
DOID:8536
  • herpes zoster
  • Aliases:
    • Shingles
    • herpes zona
Homo sapiens (human)
DOID:13001
  • carotid stenosis
  • Aliases:
    • Carotid artery stenosis
    • Stenosis, carotid artery
Homo sapiens (human)
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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: December 9, 2024