Hereditary factor II deficiency (Q89785): Difference between revisions
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A deficiência congênita de fator II é um distúrbio hemorrágico hereditário devido à redução da atividade do fator II (protrombina) e caracterizado por sintomas de sangramento mucocutâneo. A deficiência de fator II é a deficiência mais rara de fator da coagulação. | |||
| description / en | description / en | ||
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. | |||
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. |
