Systemic lupus erythematosus of childhood

disorder

SNOMED 403488004CUI C1274834

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.

Decreased serum complement C3 level

Very frequent (80-99%)HP:0005421

Decreased serum complement C4 level

Very frequent (80-99%)HP:0045042

Elevated sedimentation rate

Very frequent (80-99%)HP:0003565

Abnormality of the gastrointestinal tract

Frequent (30-79%)HP:0011024

Abnormality of the urinary system

Frequent (30-79%)HP:0000079

Absolute lymphocyte count decrease

Frequent (30-79%)HP:0001888

Antinuclear antibodies

Frequent (30-79%)HP:0003493

Antiphospholipid antibodies

Frequent (30-79%)HP:0003613

Blood in urine

Frequent (30-79%)HP:0000790

Dermatopathy

Frequent (30-79%)HP:0000951

Fluid around lungs

Frequent (30-79%)HP:0002202

Increased lactate dehydrogenase level

Frequent (30-79%)HP:0025435

Leukopenia

Frequent (30-79%)HP:0001882

Low platelet count

Frequent (30-79%)HP:0001873

Microangiopathic hemolytic anemia

Frequent (30-79%)HP:0001937

Nephritis

Frequent (30-79%)HP:0000123

Nephrosis

Frequent (30-79%)HP:0000100

Pericardial effusions

Frequent (30-79%)HP:0001698

Proteinuria

Frequent (30-79%)HP:0000093

Pyrexia

Frequent (30-79%)HP:0001945

Renal insufficiency

Frequent (30-79%)HP:0000083

Skin rash

Frequent (30-79%)HP:0000988

Soft tissue swelling

Frequent (30-79%)HP:0000969

Swollen lymph nodes

Frequent (30-79%)HP:0002716

Abnormality of the respiratory system

Occasional (5-29%)HP:0002086

Arthralgias

Occasional (5-29%)HP:0002829

Arthritis

Occasional (5-29%)HP:0001369

Ascites

Occasional (5-29%)HP:0001541

Belly bloating

Occasional (5-29%)HP:0003270

Brain and/or spinal cord issue

Occasional (5-29%)HP:0000707

Related Conditions

Systemic lupus erythematosus(parent)

Quick Facts

SNOMED CT: 403488004
UMLS CUI: C1274834
Fully Specified Name: Systemic lupus erythematosus of childhood (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.