Hereditary vitamin K-dependent coagulation factors deficiency (Q67792): Difference between revisions
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Revision as of 15:37, 14 August 2026
A disease caused by genetically inherited mutations. This disease is characterised by low levels of vitamin K in the body leading to abnormalities in coagulation of the blood. This disease may present with prolonged bleeding and haemorrhaging. Confirmation is by identification of mutations through genetic testing.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1818851075 |
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| English | Hereditary vitamin K-dependent coagulation factors deficiency |
A disease caused by genetically inherited mutations. This disease is characterised by low levels of vitamin K in the body leading to abnormalities in coagulation of the blood. This disease may present with prolonged bleeding and haemorrhaging. Confirmation is by identification of mutations through genetic testing. |
