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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