Transthyretin related familial amyloid cardiomyopathy

disorder

SNOMED 715655000CUI C4275067

Overview

Transthyretin related familial amyloid cardiomyopathy 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.

Amyloid cardiomyopathy

Very frequent (80-99%)HP:0030843

EKG abnormality

Very frequent (80-99%)HP:0003115

Increased circulating NT-proBNP concentration

Very frequent (80-99%)HP:0031185

Increased circulating troponin T concentration

Very frequent (80-99%)HP:0410174

Primary atrial arrhythmia

Very frequent (80-99%)HP:0001692

Abnormal atrioventricular conduction

Frequent (30-79%)HP:0005150

Cardiac arrhythmias

Frequent (30-79%)HP:0011675

Cardiomyopathy, hypertrophic

Frequent (30-79%)HP:0001639

Increased heart size

Frequent (30-79%)HP:0001640

Reduced ejection fraction

Frequent (30-79%)HP:0012664

Restrictive cardiomyopathy

Frequent (30-79%)HP:0001723

Abnormality of enteric nervous system morphology

Occasional (5-29%)HP:0025028

Angina pectoris

Occasional (5-29%)HP:0001681

Autonomic dysregulation

Occasional (5-29%)HP:0012332

Carpal tunnel syndrome

Occasional (5-29%)HP:0012185

Cerebral vascular events

Occasional (5-29%)HP:0001297

Decreased haemoglobin

Occasional (5-29%)HP:0001903

Embolism and thrombosis

Occasional (5-29%)HP:0001907

Heart failure

Occasional (5-29%)HP:0001635

Left ventricular wall hypertrophy

Occasional (5-29%)HP:0001712

Spinal stenosis

Occasional (5-29%)HP:0003416

Tendon rupture

Occasional (5-29%)HP:0100550

Aortic stenosis

Very rare (1-4%)HP:0001650

Peripheral nerve disease

Very rare (1-4%)HP:0001271

Peripheral neuropathy

Very rare (1-4%)HP:0009830

Related Conditions

Familial restrictive cardiomyopathy(parent)

Cardiovascular system hereditary disorder(parent)

Infiltrative cardiomyopathy(parent)

Cardiac familial non-neuropathic amyloidosis(parent)

Familial transthyretin-related amyloidosis(parent)

Quick Facts

SNOMED CT: 715655000
UMLS CUI: C4275067
Fully Specified Name: Transthyretin related familial amyloid cardiomyopathy (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 25

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.