Hereditary vitamin K-dependent coagulation factors deficiency (Q67792)
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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 |
|---|---|---|---|
| default for all languages | ID_1818851075 |
||
| 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. |
Statements
CID11:ID_1818851075
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dki-india-ID_1818851075
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Concluído
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