Hemodialysis-associated amyloidosis

disorder

SNOMED 32599008CUI C0268405

Overview

Hemodialysis-associated 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.

Arthritis

Very frequent (80-99%)HP:0001369

Neck pain

Very frequent (80-99%)HP:0030833

Shoulder pain

Very frequent (80-99%)HP:0030834

Axonal loss

Frequent (30-79%)HP:0003447

Bone cyst

Frequent (30-79%)HP:0012062

Constrictive median neuropathy

Frequent (30-79%)HP:0012185

Decreased amplitude of sensory action potentials

Frequent (30-79%)HP:0007078

Decreased nerve conduction velocity

Frequent (30-79%)HP:0000762

Dysesthesia

Frequent (30-79%)HP:0012534

Pain

Frequent (30-79%)HP:0012531

Paresthesia

Frequent (30-79%)HP:0003401

Thenar abnormality

Frequent (30-79%)HP:0001227

Abnormality of the intervertebral disc

Occasional (5-29%)HP:0005108

Abnormality of the intestine

Occasional (5-29%)HP:0002242

Abnormality of the vertebral endplates

Occasional (5-29%)HP:0005106

Deglutition disorder

Occasional (5-29%)HP:0002015

Disease of the joints

Occasional (5-29%)HP:0003040

Gastrointestinal haemorrhage

Occasional (5-29%)HP:0002239

Lingual hyperplasia

Occasional (5-29%)HP:0000158

Abnormal heart rate

Very rare (1-4%)HP:0011675

Abnormality of the shoulder

Very rare (1-4%)HP:0003043

Abnormality of the sinew

Very rare (1-4%)HP:0100261

Amyloid cardiomyopathy

Very rare (1-4%)HP:0030843

Cardiac insufficiency

Very rare (1-4%)HP:0001635

Intestinal pseudoobstruction

Very rare (1-4%)HP:0004389

Quadriparesis

Very rare (1-4%)HP:0002273

Quadriplegia

Very rare (1-4%)HP:0002445

Related Conditions

Haemodialysis-associated secondary amyloidosis of skin(child)

Amyloidosis(parent)

Long-term disorder of dialysis(parent)

Complication of hemodialysis(parent)

Quick Facts

SNOMED CT: 32599008
UMLS CUI: C0268405
Fully Specified Name: Hemodialysis-associated amyloidosis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 27

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.