Hereditary factor VIII deficiency (Q39575): Difference between revisions
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Doença causada por uma mutação geneticamente herdada levando a uma deficiência na coagulação devida à falta de fator VIII. Essa doença é caracterizada por aumento na ocorrência de hemorragias e equimoses. A confirmação é feita por identificação de mutações por testagem genética. | |||
| description / en | description / en | ||
A disease caused by a genetically inherited mutation leading to a deficiency in clotting due to lack of factor VIII. This disease is characterised by increasing haemorrhaging and bruising. Confirmation is by identification of mutations by genetic testing. | |||
Revision as of 05:03, 13 August 2026
A disease caused by a genetically inherited mutation leading to a deficiency in clotting due to lack of factor VIII. This disease is characterised by increasing haemorrhaging and bruising. Confirmation is by identification of mutations by genetic testing.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3B10 |
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| English | Hereditary factor VIII deficiency |
A disease caused by a genetically inherited mutation leading to a deficiency in clotting due to lack of factor VIII. This disease is characterised by increasing haemorrhaging and bruising. Confirmation is by identification of mutations by genetic testing. |
