Neonatal lupus erythematosus

disorder

SNOMED 95609003CUI C0409979

Overview

Neonatal lupus erythematosus 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

Abnormality of the liver

Frequent (30-79%)HP:0001392

Dermatopathy

Frequent (30-79%)HP:0000951

Hematological abnormality

Frequent (30-79%)HP:0001871

Abnormal heart rate

Occasional (5-29%)HP:0011675

Abnormal liver enzymes

Occasional (5-29%)HP:0002910

Abnormality of the cerebral white matter

Occasional (5-29%)HP:0002500

Cheekbone rash

Occasional (5-29%)HP:0025300

Cutaneous photosensitivity

Occasional (5-29%)HP:0000992

Enlarged liver

Occasional (5-29%)HP:0002240

Epidermal hyperkeratosis

Occasional (5-29%)HP:0000962

Erythematous plaque

Occasional (5-29%)HP:0025474

Heart block

Occasional (5-29%)HP:0012722

Interruption of electrical communication between upper and lower chambers of heart

Occasional (5-29%)HP:0001678

Low number of red blood cells or haemoglobin

Occasional (5-29%)HP:0001903

Low platelet count

Occasional (5-29%)HP:0001873

Maculopapular exanthema

Occasional (5-29%)HP:0040186

Neutropoenia

Occasional (5-29%)HP:0001875

Nonsyndromal hydrocephalus

Occasional (5-29%)HP:0000238

Parakeratosis

Occasional (5-29%)HP:0001036

Skin rash

Occasional (5-29%)HP:0000988

Stretched and thinned heart muscle

Occasional (5-29%)HP:0001644

Abnormal electrophysiology of sinoatrial node origin

Very rare (1-4%)HP:0011702

Abnormality of the respiratory system

Very rare (1-4%)HP:0002086

Aplastic anemia

Very rare (1-4%)HP:0001915

Basal ganglion calcification

Very rare (1-4%)HP:0002135

Big calvaria

Very rare (1-4%)HP:0000256

Bleeding tendency

Very rare (1-4%)HP:0001892

Cardiac anomaly

Very rare (1-4%)HP:0001627

Hemolytic anaemia

Very rare (1-4%)HP:0001878

Related Conditions

Lupus erythematosus(parent)

Neonatal disease(parent)

Autoimmune connective tissue disorder(parent)

Quick Facts

SNOMED CT: 95609003
UMLS CUI: C0409979
Fully Specified Name: Neonatal lupus erythematosus (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.