Congenital or constitutional haemorrhagic condition (Q58801): Difference between revisions
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CID11:ID_1181865707 | |||||||||||||||
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dki-india-ID_1181865707 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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13 August 2026
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Latest revision as of 06:22, 14 August 2026
A condition caused by determinants arising during the antenatal period or genetically inherited factors, leading to defects in clotting mechanisms or abnormalities causing structural flaws in the blood vessels. This disease is characterised by spontaneous bleeding or bruising.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1181865707 |
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| English | Congenital or constitutional haemorrhagic condition |
A condition caused by determinants arising during the antenatal period or genetically inherited factors, leading to defects in clotting mechanisms or abnormalities causing structural flaws in the blood vessels. This disease is characterised by spontaneous bleeding or bruising. |
Statements
CID11:ID_1181865707
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dki-india-ID_1181865707
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Concluído
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13 August 2026
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