3B10 Hereditary factor VIII deficiency

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

A disease caused by a genetically inherited mutation leading to a deficiency in clotting due to lack of factor VIII. This disease is characterised by increasing haemorrhaging and bruising. Confirmation is by identification of mutations by genetic testing.

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

• Haemophilia A  (3B10.0)
• Hereditary factor VIII deficiency with anti-factor VIII inhibitor  (3B10.1)
• Other specified hereditary factor VIII deficiency  (3B10.Y)
• Hereditary factor VIII deficiency, unspecified  (3B10.Z)

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