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3B13 Haemophilia C

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

A disease caused by genetically inherited mutations. This disease is characterised by decreased levels of factor XI leading to abnormalities in coagulation of the blood. This disease may present with prolonged bleeding, easy bruising or bleeding gums. Confirmation is by identification of mutation through genetic testing.

synonyms

• Haemophilia C
• Rosenthal factor deficiency
• Rosenthal syndrome
• plasma thromboplastin antecedent deficiency
• thromboplastin antecedent deficiency
• PTA - [plasma thromboplastin antecedent] deficiency
• congenital factor XI deficiency
• congenital factor XI deficiency disease
• factor XI deficiency
• hereditary factor XI deficiency disease
• Rosenthal disease

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