3B14 Other inherited coagulation factor deficiency with bleeding tendency

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

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.

sections/codes in this section (3B14-3B14)

• Hereditary deficiency of factor I  (3B14.0)
• Hereditary factor X deficiency  (3B14.1)
• Combined deficiency of vitamin K-dependent clotting factors  (3B14.2)
• Other inherited coagulation factor deficiency with bleeding tendency, unspecified  (3B14.Z)

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