Autosomal dominant beta2-microglobulinic amyloidosis

disorder

SNOMED 722292000CUI C4302669

Overview

Autosomal dominant beta2-microglobulinic 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.

CKD

Frequent (30-79%)HP:0012622

Constrictive median neuropathy

Frequent (30-79%)HP:0012185

Renal amyloidosis

Frequent (30-79%)HP:0001917

Abnormal vascular morphology

Occasional (5-29%)HP:0025015

Abnormality of muscle morphology

Occasional (5-29%)HP:0011805

Amyloid cardiomyopathy

Occasional (5-29%)HP:0030843

Amyloidosis of peripheral nerves

Occasional (5-29%)HP:0100292

Autonomic dysregulation

Occasional (5-29%)HP:0012332

Cardiovascular calcification

Occasional (5-29%)HP:0011915

Cutaneous amyloidosis

Occasional (5-29%)HP:0012309

Death of digestive organ tissue due to poor blood supply

Occasional (5-29%)HP:0005244

Glossal abnormality

Occasional (5-29%)HP:0000157

Hepatic amyloidosis

Occasional (5-29%)HP:0012280

Hip arthralgia

Occasional (5-29%)HP:0003365

Intestinal perforation

Occasional (5-29%)HP:0031368

Knee pain

Occasional (5-29%)HP:0030839

Multiple bony cystic lesions

Occasional (5-29%)HP:0012065

Nerve damage causing decreased feeling and movement

Occasional (5-29%)HP:0007141

Pathologic fracture

Occasional (5-29%)HP:0002756

Reduced ejection fraction

Occasional (5-29%)HP:0012664

Salivary gland disease

Occasional (5-29%)HP:0010286

Shoulder pain

Occasional (5-29%)HP:0030834

Spinal cord compression

Occasional (5-29%)HP:0002176

Wrist pain

Occasional (5-29%)HP:0030836

Related Conditions

Autosomal dominant hereditary disorder(parent)

Hereditary amyloidosis(parent)

Hereditary metabolic disease(parent)

Quick Facts

SNOMED CT: 722292000
UMLS CUI: C4302669
Fully Specified Name: Autosomal dominant beta2-microglobulinic amyloidosis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 24

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.