Treatments & Interventions
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Abnormal electromyography finding
Very frequent (80-99%)HP:0003457
Abnormality of the eyelids
Very frequent (80-99%)HP:0000492
Autoimmunity
Very frequent (80-99%)HP:0002960
Erythema
Very frequent (80-99%)HP:0010783
Inflammatory myopathy
Very frequent (80-99%)HP:0009071
Limb-girdle muscle weakness
Very frequent (80-99%)HP:0003325
Muscle pain
Very frequent (80-99%)HP:0003326
Periorbital edema
Very frequent (80-99%)HP:0100539
Proximal neurogenic muscle weakness
Very frequent (80-99%)HP:0003701
Water retention
Very frequent (80-99%)HP:0000969
Abnormal hair quantity
Frequent (30-79%)HP:0011362
Abnormal liver enzymes
Frequent (30-79%)HP:0002910
Anti-SAE 2 antibody positivity
Frequent (30-79%)HP:0034141
Anti-SUMO-activating enzyme subunit 1 antibody positivity
Frequent (30-79%)HP:0034140
Arthritic pain
Frequent (30-79%)HP:0002829
Arthritis
Frequent (30-79%)HP:0001369
Calcium deposits in joints
Frequent (30-79%)HP:0000934
Central hypotonia
Frequent (30-79%)HP:0001252
Diffuse reticular or finely nodular infiltrations
Frequent (30-79%)HP:0002207
Elevated circulating aldolase concentration
Frequent (30-79%)HP:0012544
Elevated circulating creatine phosphokinase
Frequent (30-79%)HP:0003236
EMG: myopathic changes
Frequent (30-79%)HP:0003458
Gottron papules
Frequent (30-79%)HP:0025508
Heliotrope rash
Frequent (30-79%)HP:0040324
Increased lactate dehydrogenase level
Frequent (30-79%)HP:0025435
Interstitial pulmonary disease
Frequent (30-79%)HP:0006530
Muscle inflammation
Frequent (30-79%)HP:0100614
Nail disease
Frequent (30-79%)HP:0001597
Open skin sore
Frequent (30-79%)HP:0200042
Papules
Frequent (30-79%)HP:0200034
Related Conditions
Sclerodermatomyositis(child)
Dermatopolymyositis in neoplastic disease(child)
Idiopathic dermatomyositis(child)
Childhood type dermatomyositis(child)
Poikilodermatomyositis(child)
Adult onset dermatomyositis(child)
Drug-induced dermatomyositis(child)
Neonatal dermatomyositis(child)
Dermatomyositis overlap syndrome(child)
Inflammatory dermatosis(parent)
Myositis(parent)
Quick Facts
- SNOMED CT
- 396230008
- UMLS CUI
- C0011633
- Fully Specified Name
- Dermatomyositis (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
- Known Treatments
- 3
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.