Haemophilia C (Q39580): Difference between revisions
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dki-india-3B13 | |||||||||||||||
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13 August 2026
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Latest revision as of 05:03, 13 August 2026
A disease caused by genetically inherited mutations. This disease is characterised by decreased levels of factor XI leading to abnormalities in coagulation of the blood. This disease may present with prolonged bleeding, easy bruising or bleeding gums. Confirmation is by identification of mutation through genetic testing.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3B13 |
||
| English | Haemophilia C |
A disease caused by genetically inherited mutations. This disease is characterised by decreased levels of factor XI leading to abnormalities in coagulation of the blood. This disease may present with prolonged bleeding, easy bruising or bleeding gums. Confirmation is by identification of mutation through genetic testing. |
Statements
CID11:3B13
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dki-india-3B13
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Concluído
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13 August 2026
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