Primary familial hypertrophic cardiomyopathy

disorder

SNOMED 83978005CUI C0949658

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Asymmetric septal hypertrophy

HP:0001670

Cardiac arrhythmias

HP:0011675

Heart failure

HP:0001635

Narrowing of blood vessel below aortic heart valve

HP:0001682

Sudden death

HP:0001699

Related Conditions

Familial cardiomyopathy(parent)

Primary hypertrophic cardiomyopathy(parent)

Quick Facts

SNOMED CT: 83978005
UMLS CUI: C0949658
Fully Specified Name: Primary familial hypertrophic cardiomyopathy (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 5

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.