Inherited coagulation factor deficiency without bleeding tendency (Q39583): Difference between revisions
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13 August 2026
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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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 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. |
Statements
CID11:3B15
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dki-india-3B15
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Concluído
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13 August 2026
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