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Eosinophilic myositis

disorder
SNOMED 370474006CUI C1299884

Overview

Eosinophilic myositis 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.

Elevated circulating creatine phosphokinase
Always present (100%)HP:0003236
Eosinophilic infiltration of skeletal muscle
Always present (100%)HP:0032019
Clumsiness
Frequent (30-79%)HP:0002312
Eosinophilia
Frequent (30-79%)HP:0001880
Lower limb muscle weakness
Frequent (30-79%)HP:0007340
Facial muscle weakness of muscles innervated by CN VII
Occasional (5-29%)HP:0010628
Congenital muscular dystrophy
HP:0003560
Flexion contractures
HP:0001371
Gait disturbance
HP:0001288
Muscle inflammation
HP:0100614
Scapula alata
HP:0003691
Symmetrical, proximal limb muscle atrophy
HP:0007126

Quick Facts

SNOMED CT
370474006
UMLS CUI
C1299884
Fully Specified Name
Eosinophilic myositis (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
12
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.