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3B15 Inherited coagulation factor deficiency without bleeding tendency

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

A disease caused by a genetically inherited mutation leading to decreased levels of coagulation factor. This disease is characterised by decreased levels of coagulation factor without leading to increased haemorrhaging. Confirmation is by identification of decreased levels of coagulation factor in a blood sample.

synonyms

• Inherited coagulation factor deficiency without bleeding tendency
• Congenital prekallikrein deficiency
• Congenital high-molecular-weight kininogen deficiency
• Hereditary factor XII deficiency
• Congenital Hageman factor deficiency
• congenital factor XII deficiency
• Deficiency of factor XII
• factor XII deficiency disease
• Hageman defect
• Hageman deficiency
• Hageman factor defect
• Hageman factor deficiency

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