Hemorrhagic Disease

Alias:
Hemorrhagic Disorders
Haemorrhagic Disorder Due to Excess Administered Heparin
Acquired Coagulation Factor Inhibitor Disorder
Haemorrhagic Disorder Due to Antithrombinaemia
Haemorrhagic Disorder Due to Hyperheparinemia
Circulating Anticoagulant Disorder
Acquired Inhibitor of Coagulation
Antithromboplastinogenaemia
Antithromboplastinaemia
Hemorrhagic Diathesis
Hemorrhagic Diseases
Bleeding Tendency
Antithrombinaemia
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hemorrhagic Disease, also known as hemorrhagic disorders, is related to vitamin k deficiency bleeding and alpha-2-plasmin inhibitor deficiency, and has symptoms including abnormal bruising, angina pectoris and chest pain. An important gene associated with Hemorrhagic Disease is F11 (Coagulation Factor XI), and among its related pathways/superpathways are Response to elevated platelet cytosolic Ca2+ and Collagen chain trimerization. The drugs Protective Agents and Charcoal have been mentioned in the context of this disorder. Affiliated tissues include prostate and endothelial, and related phenotypes are homeostasis/metabolism and cardiovascular system
Related ID:
MESH:D006474
ICD11:156218529

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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33
265
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Medical Symptom

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Description
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Gene & Mutation

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Related Drugs

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Disease Model

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MGI
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References Literature

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