Hereditary factor VIII deficiency (Q39575)
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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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3B10 |
||
| English | Hereditary factor VIII deficiency |
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. |
Statements
CID11:3B10
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dki-india-3B10
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Concluído
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13 August 2026
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