Congenital non-inherited haemorrhagic condition (Q62069): Difference between revisions
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Condição causada por determinantes que surgem no período pré-natal e que levam a defeitos nos mecanismos de coagulação ou a anormalidades que causam um defeito estrutural nos vasos sanguíneos. Essa condição é caraterizada por sangramentos ou equimoses espontâneas. | |||
| description / en | description / en | ||
A condition caused by determinants arising during the antenatal period, leading to defects in clotting mechanisms or abnormalities causing a structural flaw in the blood vessels. This condition is characterised by spontaneous bleeding or bruising. | |||
Revision as of 09:34, 14 August 2026
A condition caused by determinants arising during the antenatal period, leading to defects in clotting mechanisms or abnormalities causing a structural flaw in the blood vessels. This condition is characterised by spontaneous bleeding or bruising.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_165588496 |
||
| English | Congenital non-inherited haemorrhagic condition |
A condition caused by determinants arising during the antenatal period, leading to defects in clotting mechanisms or abnormalities causing a structural flaw in the blood vessels. This condition is characterised by spontaneous bleeding or bruising. |
