Hereditary factor II deficiency (Q89785): Difference between revisions
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13 August 2026
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Latest revision as of 16:37, 15 August 2026
Congenital factor II deficiency is an inherited bleeding disorder due to reduced activity of factor II (FII, prothrombin) and characterised by mucocutaneous bleeding symptoms. Factor II deficiency is the most rare coagulation factor deficiency.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1522212461 |
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| English | Hereditary factor II deficiency |
Congenital factor II deficiency is an inherited bleeding disorder due to reduced activity of factor II (FII, prothrombin) and characterised by mucocutaneous bleeding symptoms. Factor II deficiency is the most rare coagulation factor deficiency. |
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CID11:ID_1522212461
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dki-india-ID_1522212461
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Concluído
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13 August 2026
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