Autoimmune necrotizing myopathy

disorder

SNOMED 715863001CUI C3267047

Overview

Autoimmune necrotizing myopathy 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.

Autoimmune antibody positivity

Very frequent (80-99%)HP:0030057

Elevated serum creatine phosphokinase

Very frequent (80-99%)HP:0003236

EMG: myopathic changes

Very frequent (80-99%)HP:0003458

Fatiguable weakness of proximal limb muscles

Very frequent (80-99%)HP:0030200

Muscle fibre necrosis

Very frequent (80-99%)HP:0003713

Myopathy

Very frequent (80-99%)HP:0003198

Anti-3-hydroxy- 3-methylglutaryl-coA reductase antibody positivity

Frequent (30-79%)HP:0033708

Anti-signal recognition particle antibody positivity

Frequent (30-79%)HP:0033713

Deglutition disorder

Frequent (30-79%)HP:0002015

Muscle degeneration

Frequent (30-79%)HP:0003202

Muscle inflammation

Frequent (30-79%)HP:0100614

Muscle pain

Frequent (30-79%)HP:0003326

Proximal muscle weakness in lower limbs

Frequent (30-79%)HP:0008994

Axial muscle weakness

Occasional (5-29%)HP:0003327

Cancer

Occasional (5-29%)HP:0002664

Chest pain

Occasional (5-29%)HP:0100749

Inflammation of heart muscle

Occasional (5-29%)HP:0012819

Interstitial pulmonary disease

Occasional (5-29%)HP:0006530

Palpitations

Occasional (5-29%)HP:0001962

Scapula alata

Occasional (5-29%)HP:0003691

Arthralgias

Very rare (1-4%)HP:0002829

Chronic heart failure

Very rare (1-4%)HP:0001635

Raynaud phenomenon

Very rare (1-4%)HP:0030880

Skin rash

Very rare (1-4%)HP:0000988

Related Conditions

Idiopathic inflammatory myopathy(parent)

Autoimmune inflammation of skeletal muscle(parent)

Injury of musculoskeletal system(parent)

Injury of muscle(parent)

Soft tissue injury(parent)

Lesion of skeletal muscle(parent)

Tissue necrosis(parent)

Quick Facts

SNOMED CT: 715863001
UMLS CUI: C3267047
Fully Specified Name: Autoimmune necrotizing myopathy (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.