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Hemorrhagic disease

Spontaneous or near spontaneous bleeding caused by a defect in clotting mechanisms (blood coagulation disorders) or another abnormality causing a structural flaw in the blood vessels (hemostatic disorders).

Identifiers
MONDO:0002243
Part of
Hematologic disorder
Also known as
bleeding diathesis · bleeding disorder · bleeding predisposition · bleeding tendency

Subtypes

All diseases Rare only
Disease Subtypes
Inherited bleeding disorder, platelet-type 49
Hereditary von Willebrand disease 11
Vascular hemostatic disease 10
Purpura 8
Congenital fibrinogen deficiency 5
Congenital vitamin K-dependent coagulation factors deficiency 5
Hemophilia A 5
Hemophilia B 4
Acquired hemophilia 3
Combined deficiency of factor V and factor VIII 3
Fetal and neonatal alloimmune thrombocytopenia 3
Congenital factor XIII deficiency 2
Factor VII deficiency 2
Factor X deficiency 2
Prothrombin deficiency 2
East Texas bleeding disorder
Acquired von willebrand syndrome
Alpha-2-plasmin inhibitor deficiency
Congenital factor V deficiency
Congenital factor XI deficiency
Congenital factor XII deficiency
Congenital high-molecular-weight kininogen deficiency
Congenital plasminogen activator inhibitor type 1 deficiency
Hemophilia B leyden
Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation
Inherited prekallikrein deficiency
Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome
Thrombomodulin-related bleeding disorder

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