Familial pulmonary arterial hypertension due to BMPR2 mutations (Q104308): Difference between revisions

From determinar.ia.br - Determine suas informações
‎Changed an Item
‎Changed an Item
 
(2 intermediate revisions by the same user not shown)
Property / Verification Status
 
Concluído
Property / Verification Status: Concluído / rank
 
Normal rank
Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
Normal rank
Property / Collection date
 
16 August 2026
Timestamp+2026-08-16T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 16 August 2026 / rank
 
Normal rank

Latest 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
    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.

      Statements

      CID11:ID_301374783
      0 references
      dki-india-ID_301374783
      0 references
      Concluído
      0 references
      16 August 2026
      0 references