Haemophilia C (Q39580): Difference between revisions
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Doença causada por mutações geneticamente herdadas. Essa doença é caracterizada por níveis diminuídos de fator XI, levando a anormalidades da coagulação sanguínea. Essa doença pode apresentar-se com sangramento prolongado, hematomas espontâneos, ou gengivorragia. A confirmação é feita pela identificação da mutação por testagem genética. | |||
| description / en | description / en | ||
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. | |||
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. |
