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Congenital or constitutional haemorrhagic condition

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

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.

sections/codes in this section (3B10-3B1Z)

• Hereditary factor VIII deficiency  (3B10)
• Hereditary factor IX deficiency  (3B11)
• Von Willebrand disease  (3B12)
• Haemophilia C  (3B13)
• Other inherited coagulation factor deficiency with bleeding tendency  (3B14)
• Inherited coagulation factor deficiency without bleeding tendency  (3B15)
• Congenital or constitutional haemorrhagic condition, unspecified  (3B1Z)

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