Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation

disorder

SNOMED 766883006CUI C4707865

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.

Abnormality of cardiac conduction system

Very frequent (80-99%)HP:0031546

Stretched and thinned heart muscle

Very frequent (80-99%)HP:0001644

Abnormal myocardium morphology

Frequent (30-79%)HP:0001637

Inability to make and keep healthy fat tissue

Frequent (30-79%)HP:0009125

Left ventricular impairment

Frequent (30-79%)HP:0005162

Quivering upper heart chambers resulting in irregular heartbeat

Frequent (30-79%)HP:0005110

Sudden cardiac death

Frequent (30-79%)HP:0001645

Syncope

Frequent (30-79%)HP:0001279

Abnormal lymphocyte physiology

Occasional (5-29%)HP:0031409

Atrial flutter

Occasional (5-29%)HP:0004749

Congenital muscular dystrophy

Occasional (5-29%)HP:0003560

Heart block

Occasional (5-29%)HP:0012722

Heart failure

Occasional (5-29%)HP:0001635

Pericardial effusions

Occasional (5-29%)HP:0001698

Sinoatrial block

Occasional (5-29%)HP:0012723

Supraventricular tachyarrhythmia

Occasional (5-29%)HP:0004755

Ventricular arrhythmias

Occasional (5-29%)HP:0004308

Related Conditions

Familial cardiomyopathy(parent)

Cardiovascular system hereditary disorder(parent)

Congestive cardiomyopathy(parent)

Conduction disorder of the heart(parent)

Autosomal dominant hereditary disorder(parent)

Quick Facts

SNOMED CT: 766883006
UMLS CUI: C4707865
Fully Specified Name: Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 17

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.