Senile systemic amyloidosis

disorder

SNOMED 237877004CUI C0342623

Overview

Senile systemic amyloidosis 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.

Abnormal lung parenchyma morphology

Very frequent (80-99%)HP:0006530

Cardiac insufficiency

Very frequent (80-99%)HP:0001635

Cardiomyopathy, hypertrophic

Very frequent (80-99%)HP:0001639

EKG abnormality

Very frequent (80-99%)HP:0003115

Excess fluid in lungs

Very frequent (80-99%)HP:0100598

Fluid around lungs

Very frequent (80-99%)HP:0002202

Myocardial infarction

Very frequent (80-99%)HP:0001658

Pedal oedema

Very frequent (80-99%)HP:0010741

Transthyretin cardiac amyloidosis

Very frequent (80-99%)HP:0031327

Anal incontinence

Frequent (30-79%)HP:0002607

Autonomic bladder dysfunction

Frequent (30-79%)HP:0005341

Autonomic dysregulation

Frequent (30-79%)HP:0012332

Cardiac arrhythmias

Frequent (30-79%)HP:0011675

Chronic diarrhoea

Frequent (30-79%)HP:0002028

Constrictive median neuropathy

Frequent (30-79%)HP:0012185

Decreased or absent ankle reflexes

Frequent (30-79%)HP:0200101

Elevated alkaline phosphatase

Frequent (30-79%)HP:0003155

Enlarged liver

Frequent (30-79%)HP:0002240

GI dysmotility

Frequent (30-79%)HP:0002579

Impaired vibratory sensation

Frequent (30-79%)HP:0002495

Intermittent diarrhea

Frequent (30-79%)HP:0002254

Orthostatic hypotension due to autonomic dysfunction

Frequent (30-79%)HP:0004926

Quivering upper heart chambers resulting in irregular heartbeat

Frequent (30-79%)HP:0005110

Sensory neuropathy

Frequent (30-79%)HP:0000763

Aortic stenosis

Occasional (5-29%)HP:0001650

Bradycardia

Occasional (5-29%)HP:0001662

Kidney disease

Occasional (5-29%)HP:0000112

Nephrosis

Occasional (5-29%)HP:0000100

Proteinuria

Occasional (5-29%)HP:0000093

Renal insufficiency

Occasional (5-29%)HP:0000083

Related Conditions

Systemic amyloidosis(parent)

Age-related amyloidosis(parent)

Quick Facts

SNOMED CT: 237877004
UMLS CUI: C0342623
Fully Specified Name: Wild type ATTR amyloidosis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 30

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.