Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation

disorder

SNOMED 697900005CUI C3697369

Overview

Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation is a disorder.

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

Related Conditions

Heritable pulmonary arterial hypertension(parent)

Quick Facts

SNOMED CT: 697900005
UMLS CUI: C3697369
Fully Specified Name: Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin 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.