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AGEP - acute generalised exanthematous pustulosis
disorderSNOMED 702617007CUI C0877055
Overview
AGEP - acute generalised exanthematous pustulosis 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.
Increased total leukocyte count
Very frequent (80-99%)HP:0001974
Pustules
Very frequent (80-99%)HP:0200039
Elevated sedimentation rate
Frequent (30-79%)HP:0003565
Eosinophilia
Frequent (30-79%)HP:0001880
Eosinophilic dermatitis
Frequent (30-79%)HP:0032022
Neutrophilia
Frequent (30-79%)HP:0011897
Pyrexia
Frequent (30-79%)HP:0001945
Scaling skin
Frequent (30-79%)HP:0040189
Skin itching
Frequent (30-79%)HP:0000989
Abnormal liver function
Occasional (5-29%)HP:0002910
Facial swelling
Occasional (5-29%)HP:0000282
Nikolsky's sign
Occasional (5-29%)HP:0100792
Panting
Occasional (5-29%)HP:0002094
Predominantly dermal neutrophilic infiltrate
Occasional (5-29%)HP:0031236
Red and sore lips
Occasional (5-29%)HP:0100825
Red or purple spots on the skin
Occasional (5-29%)HP:0000979
Renal failure
Occasional (5-29%)HP:0000083
Skin vesicle
Occasional (5-29%)HP:0200037
Slowed or blocked flow of bile from liver
Occasional (5-29%)HP:0001396
Conjunctivitis, recurrent
Very rare (1-4%)HP:0000509
Lymph node hyperplasia
Very rare (1-4%)HP:0002716
Melanoderma
Very rare (1-4%)HP:0000953
Neutropoenia
Very rare (1-4%)HP:0001875
Quick Facts
- SNOMED CT
- 702617007
- UMLS CUI
- C0877055
- Fully Specified Name
- Acute generalized exanthematous pustulosis (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 23
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.