Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Friedreich's ataxia
Frequent (30-79%)
AL amyloidosis
Frequent (30-79%)
African trypanosomiasis
Frequent (30-79%)
Dextrocardia
Very frequent (80-99%)
Duchenne muscular dystrophy
Trypanosomiasis
Frequent (30-79%)
Agenesis of pulmonary artery
Frequent (30-79%)
Cardiogenic shock
Very frequent (80-99%)
Turner's phenotype, karyotype normal
Very frequent (80-99%)
Noonan's syndrome
Very frequent (80-99%)
Early onset cerebellar ataxia with retained tendon reflexes
Occasional (5-29%)
Senile systemic amyloidosis
Very frequent (80-99%)
Dopamine beta-hydroxylase deficiency
Occasional (5-29%)
Complete atrioventricular septal defect
Very frequent (80-99%)
Coronary artery fistula
Frequent (30-79%)
Becker muscular dystrophy
Connective tissue disease overlap syndrome
Occasional (5-29%)
Mixed collagen vascular disease
Occasional (5-29%)
Acquired thrombotic thrombocytopenic purpura
Occasional (5-29%)
Idiopathic neonatal atrial flutter
Very frequent (80-99%)
Tropical endomyocardial fibrosis
Very frequent (80-99%)
Transthyretin related familial amyloid cardiomyopathy
Very frequent (80-99%)
Deafness with cataract and skeletal anomaly syndrome
Autosomal recessive limb girdle muscular dystrophy type 2B
Occasional (5-29%)
Congenital cardiac diverticulum
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 102594003
- UMLS CUI
- C0522055
- Fully Specified Name
- Electrocardiogram abnormal (finding)
- Associated Conditions
- 25
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.