Progressive familial heart block

disorder

SNOMED 698249005CUI C1879286

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.

Abnormal heart rate

Frequent (30-79%)HP:0011675

Bundle branch block

Frequent (30-79%)HP:0011710

Chronic heart failure

Frequent (30-79%)HP:0001635

Gastro pain

Frequent (30-79%)HP:0002027

Heart block

Frequent (30-79%)HP:0012722

Lengthened PR interval on EKG

Frequent (30-79%)HP:0012248

Panting

Frequent (30-79%)HP:0002094

Right bundle-branch block

Frequent (30-79%)HP:0011712

Syncope

Frequent (30-79%)HP:0001279

Vertigo

Frequent (30-79%)HP:0002321

Left anterior hemiblock

Occasional (5-29%)HP:0011711

Left posterior fascicular block

Occasional (5-29%)HP:0005172

Complete heart block with broad QRS complexes

HP:0005170

Sudden cardiac death

HP:0001645

Sudden death

HP:0001699

Related Conditions

Lev's disease(child)

Progressive familial heart block, type IB(child)

Progressive familial heart block, type II(child)

Heart block(parent)

Quick Facts

SNOMED CT: 698249005
UMLS CUI: C1879286
Fully Specified Name: Progressive familial heart block (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 15

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.