Other inherited coagulation factor deficiency with bleeding tendency (Q39584): Difference between revisions

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Qualquer doença causada por mutações geneticamente herdadas levando à falta de fatores da coagulação no sangue não classificada em outra parte. Essas doenças são caracterizadas pela ocorrência aumentada de hemorragias e equimoses, pois o sangue não coagula adequadamente para controlar o sangramento. A confirmação é feita pela identificação de mutações por testagem genética.
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Any disease caused by genetically inherited mutations leading to lack of coagulation factors in the blood not elsewhere classified. These diseases are characterised by increased haemorrhaging and bruising as the blood cannot clot properly to control bleeding. Confirmation is identification of mutations by genetic testing.

Revision as of 05:03, 13 August 2026

Any disease caused by genetically inherited mutations leading to lack of coagulation factors in the blood not elsewhere classified. These diseases are characterised by increased haemorrhaging and bruising as the blood cannot clot properly to control bleeding. Confirmation is identification of mutations by genetic testing.
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3B14
    English
    Other inherited coagulation factor deficiency with bleeding tendency
    Any disease caused by genetically inherited mutations leading to lack of coagulation factors in the blood not elsewhere classified. These diseases are characterised by increased haemorrhaging and bruising as the blood cannot clot properly to control bleeding. Confirmation is identification of mutations by genetic testing.

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