Childhood type dermatomyositis

disorder

SNOMED 1212005CUI C0263666

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Autoimmune disorder

Very frequent (80-99%)HP:0002960

Calcinosis

Very frequent (80-99%)HP:0003761

Elevated C-reactive protein level

Very frequent (80-99%)HP:0011227

Elevated circulating creatine phosphokinase

Very frequent (80-99%)HP:0003236

Elevated sedimentation rate

Very frequent (80-99%)HP:0003565

Erythema

Very frequent (80-99%)HP:0010783

Mucosal telangiectasiae

Very frequent (80-99%)HP:0100579

Muscle inflammation

Very frequent (80-99%)HP:0100614

Muscle pain

Very frequent (80-99%)HP:0003326

Muscle weakness

Very frequent (80-99%)HP:0001324

Skin rash

Very frequent (80-99%)HP:0000988

Swelling of eyelids

Very frequent (80-99%)HP:0100540

Teleangiectasia of the skin

Very frequent (80-99%)HP:0100585

Tiredness

Very frequent (80-99%)HP:0012378

Xerosis

Very frequent (80-99%)HP:0000958

Arthralgias

Frequent (30-79%)HP:0002829

Arthritis

Frequent (30-79%)HP:0001369

Cutaneous photosensitivity

Frequent (30-79%)HP:0000992

Dyschezia

Frequent (30-79%)HP:0002019

Hair loss

Frequent (30-79%)HP:0001596

Inflammation of blood vessel

Frequent (30-79%)HP:0002633

Muscle spasm

Frequent (30-79%)HP:0003394

Muscular hypotonia

Frequent (30-79%)HP:0001252

Open skin sore

Frequent (30-79%)HP:0200042

Poikiloderma

Frequent (30-79%)HP:0001029

Pyrexia

Frequent (30-79%)HP:0001945

Restrictive lung disease

Frequent (30-79%)HP:0002091

Skin itching

Frequent (30-79%)HP:0000989

Abnormal electromyography finding

Occasional (5-29%)HP:0003457

Abnormal heart rate

Occasional (5-29%)HP:0011675

Related Conditions

Juvenile dermatomyositis co-occurrent with respiratory involvement(child)

Hypomyopathic juvenile dermatomyositis(child)

Juvenile dermatomyositis overlap syndrome(child)

Dermatomyositis(parent)

Dermatosis in childhood(parent)

Quick Facts

SNOMED CT: 1212005
UMLS CUI: C0263666
Fully Specified Name: Childhood type dermatomyositis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 30

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.