Heritable pulmonary arterial hypertension due to BMPR2 mutation

disorder

SNOMED 697899000CUI C3698563

Overview

Heritable pulmonary arterial hypertension due to BMPR2 mutation is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Related Conditions

Heritable pulmonary arterial hypertension(parent)

Autosomal dominant hereditary disorder(parent)

Cardiovascular system hereditary disorder(parent)

Quick Facts

SNOMED CT: 697899000
UMLS CUI: C3698563
Fully Specified Name: Heritable pulmonary arterial hypertension due to bone morphogenetic protein receptor type II mutation (disorder)
Specialists: 0
Diagnostic Biomarkers: 0

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.

Heritable pulmonary arterial hypertension due to BMPR2 mutation — Symptoms, Testing & Specialists | Ltrl | Healos