- Congenital coagulopathy, genetic coagulopathy with mostly selective coagulation defect ( haemophilia, Willebrand v.-Jürgens disease)
- Acquired coagulopathy (disorders of several coagulation factors)
- vitamin K deficiency
- Hepatogenic bleeding tendency
- Uremic bleeding tendency
- Consumption coagulopathy
- Immunocoagulopathies (inhibitor formation)
- purpura hyperglobulinaemica
- Hemorrhagic diathesis of the newborn.
CoagulopathiesD68.9
DefinitionThis section has been translated automatically.
Haemorrhagic diathesis, caused by disorders of the plasmatic coagulation factors, see also Haemorrhagic diathesis. A distinction is made between: