Congenital or constitutional haemorrhagic condition

Definition

A condition caused by determinants arising during the antenatal period or genetically inherited factors, leading to defects in clotting mechanisms or abnormalities causing structural flaws in the blood vessels. This disease is characterised by spontaneous bleeding or bruising.

8 subordinate codes

• 3B10Hereditary factor VIII deficiency
• 3B11Hereditary factor IX deficiency
• 3B12Von Willebrand disease
• 3B13Haemophilia C
• 3B14Other inherited coagulation factor deficiency with bleeding tendency
• 3B15Inherited coagulation factor deficiency without bleeding tendency
• Congenital non-inherited haemorrhagic condition
• 4B4ZDiseases of the immune system, unspecified

Nearby in Coagulation defects

• 3B20-3B2YHaemorrhagic diseases due to acquired coagulation factor defects
• 4B4ZDiseases of the immune system, unspecified