Other inherited coagulation factor deficiency with bleeding tendency

Definition

Any disease caused by genetically inherited mutations leading to lack of coagulation factors in the blood not elsewhere classified. These diseases are characterised by increased haemorrhaging and bruising as the blood cannot clot properly to control bleeding. Confirmation is identification of mutations by genetic testing.

4 subordinate codes

• 3B14.0Hereditary deficiency of factor I
• 3B14.1Hereditary factor X deficiency
• 3B14.2Combined deficiency of vitamin K-dependent clotting factors
• 4B4ZDiseases of the immune system, unspecified

Nearby in Congenital or constitutional haemorrhagic condition

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