Inherited coagulation factor deficiency without bleeding tendency (Q39583): Difference between revisions

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Doença causada por uma mutação geneticamente herdada levando a níveis diminuídos de fator da coagulação. Essa doença é caracterizada por níveis diminuídos de fator da coagulação sem levar a aumento de hemorragias. A confirmação é feita pela identificação de níveis diminuídos de fator da coagulação em amostra de sangue.
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A disease caused by a genetically inherited mutation leading to decreased levels of coagulation factor. This disease is characterised by decreased levels of coagulation factor without leading to increased haemorrhaging. Confirmation is by identification of decreased levels of coagulation factor in a blood sample.

Revision as of 05:03, 13 August 2026

A disease caused by a genetically inherited mutation leading to decreased levels of coagulation factor. This disease is characterised by decreased levels of coagulation factor without leading to increased haemorrhaging. Confirmation is by identification of decreased levels of coagulation factor in a blood sample.
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3B15
    English
    Inherited coagulation factor deficiency without bleeding tendency
    A disease caused by a genetically inherited mutation leading to decreased levels of coagulation factor. This disease is characterised by decreased levels of coagulation factor without leading to increased haemorrhaging. Confirmation is by identification of decreased levels of coagulation factor in a blood sample.

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