hemorrhagic disease
MONDO:0002243Mondo
Findings
No curated finding names hemorrhagic disease yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
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).
Definition from the Mondo Disease Ontology (MONDO:0002243), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
- Narrower terms (28)
- acquired hemophilia
- acquired von willebrand syndrome
- alpha-2-plasmin inhibitor deficiency
- combined deficiency of factor V and factor VIII
- congenital factor V deficiency
- congenital factor XI deficiency
- congenital factor XII deficiency
- congenital factor XIII deficiency
- congenital fibrinogen deficiency
- congenital high-molecular-weight kininogen deficiency
- congenital plasminogen activator inhibitor type 1 deficiency
- congenital vitamin K-dependent coagulation factors deficiency
- East Texas bleeding disorder
- factor VII deficiency
- factor X deficiency
- fetal and neonatal alloimmune thrombocytopenia
- hemophilia A
- hemophilia B
- hemophilia B leyden
- hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation
- hereditary von Willebrand disease
- inherited bleeding disorder, platelet-type
- inherited prekallikrein deficiency
- multiple sclerosis-ichthyosis-factor VIII deficiency syndrome
- prothrombin deficiency
- purpura
- thrombomodulin-related bleeding disorder
- vascular hemostatic disease
Other names
4 names
Resolves to: hemorrhagic disease
- Also called
- bleeding diathesisbleeding disorderbleeding predispositionbleeding tendency