Familial idiopathic dilatation of right atrium

disorder

SNOMED 716773002CUI C4274283

Overview

Familial idiopathic dilatation of right atrium is a disorder.

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

Signs & Symptoms

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

Atrial septal aneurysm

Very frequent (80-99%)HP:0011995

Dilated right atrium

Very frequent (80-99%)HP:0030718

Abnormal cardiac ventricular function

Frequent (30-79%)HP:0030872

Abnormal heart rate

Frequent (30-79%)HP:0011675

Abnormality of liver blood vessels

Frequent (30-79%)HP:0006707

Abnormality of the vena cava

Frequent (30-79%)HP:0005345

Complete heart block with narrow QRS complexes

Frequent (30-79%)HP:0005178

Holosystolic murmur

Frequent (30-79%)HP:0031667

Increased heart size

Frequent (30-79%)HP:0001640

Interruption of electrical communication between upper and lower chambers of heart

Frequent (30-79%)HP:0001678

Midsystolic murmur

Frequent (30-79%)HP:0031665

Panting

Frequent (30-79%)HP:0002094

Quivering upper heart chambers resulting in irregular heartbeat

Frequent (30-79%)HP:0005110

Reduced ejection fraction

Frequent (30-79%)HP:0012664

Right ventricular hypertrophy

Frequent (30-79%)HP:0001667

Skipped heart beat

Frequent (30-79%)HP:0001962

Syncope

Frequent (30-79%)HP:0001279

Tricuspid regurgitation

Frequent (30-79%)HP:0005180

Abnormal jugular vein morphology

Occasional (5-29%)HP:3000042

Enlarged liver

Occasional (5-29%)HP:0002240

Epilepsy

Occasional (5-29%)HP:0001250

Fluid around lungs

Occasional (5-29%)HP:0002202

Intermittent atrial fibrillation

Occasional (5-29%)HP:0004757

Peripheral edema

Occasional (5-29%)HP:0012398

Related Conditions

Idiopathic disease(parent)

Congenital dilatation of atrium(parent)

Familial disease(parent)

Right atrial dilatation(parent)

Congenital abnormality of right atrium(parent)

Quick Facts

SNOMED CT: 716773002
UMLS CUI: C4274283
Fully Specified Name: Familial idiopathic dilatation of right atrium (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 24

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.