Familial pulmonary arterial hypertension due to BMPR2 mutations (Q104308): Difference between revisions
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Aumento familiar da pressão arterial na artéria pulmonar, veia pulmonar ou capilares pulmonares, conjuntamente conhecidos como vasculatura pulmonar, levando a falta de ar, tontura, desmaio e outros sintomas, todos estes exacerbados pelo esforço, devido a mutações BMPR2. | |||
| description / en | description / en | ||
This is a familial increase of blood pressure in the pulmonary artery, pulmonary vein, or pulmonary capillaries, together known as the lung vasculature, leading to shortness of breath, dizziness, fainting, and other symptoms, all of which are exacerbated by exertion, due to BMPR2 mutations. | |||
Revision as of 10:10, 17 August 2026
This is a familial increase of blood pressure in the pulmonary artery, pulmonary vein, or pulmonary capillaries, together known as the lung vasculature, leading to shortness of breath, dizziness, fainting, and other symptoms, all of which are exacerbated by exertion, due to BMPR2 mutations.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_301374783 |
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| English | Familial pulmonary arterial hypertension due to BMPR2 mutations |
This is a familial increase of blood pressure in the pulmonary artery, pulmonary vein, or pulmonary capillaries, together known as the lung vasculature, leading to shortness of breath, dizziness, fainting, and other symptoms, all of which are exacerbated by exertion, due to BMPR2 mutations. |
