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Familial eosinophilia

disorder
SNOMED 79336007CUI C0272192

Overview

Familial eosinophilia 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.

Eosinophilia
Always present (100%)HP:0001880
Increased total leukocyte count
Always present (100%)HP:0001974
Lung infiltrates
Frequent (30-79%)HP:0002113
Low platelet count
Occasional (5-29%)HP:0001873
Bronchitis, recurrent
HP:0002837
Low number of red blood cells or hemoglobin
HP:0001903
Myocardial eosinophilic infiltration
HP:0031323

Quick Facts

SNOMED CT
79336007
UMLS CUI
C0272192
Fully Specified Name
Familial eosinophilia (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
7
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.