Hereditary factor VII deficiency (Q89789): Difference between revisions
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13 August 2026
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Latest revision as of 16:37, 15 August 2026
Factor VII (FVII) deficiency is a rare hereditary haemorrhagic disease caused by the diminution or absence of this coagulation factor. The clinical expression of this disorder is highly variable, and no consistent relationship has been found between the severity of the haemorrhagic syndrome and the residual levels of FVII activity.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2034923927 |
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| English | Hereditary factor VII deficiency |
Factor VII (FVII) deficiency is a rare hereditary haemorrhagic disease caused by the diminution or absence of this coagulation factor. The clinical expression of this disorder is highly variable, and no consistent relationship has been found between the severity of the haemorrhagic syndrome and the residual levels of FVII activity. |
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CID11:ID_2034923927
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dki-india-ID_2034923927
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Concluído
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13 August 2026
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