Eosinophil peroxidase deficiency

disorder

SNOMED 711160007CUI C1850000

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.

Eosinophil nuclear hypersegmentation

Always present (100%)HP:0034253

Related Conditions

Non-malignant white cell disorder(parent)

Recessive hereditary disorder (autosomal)(parent)

Quick Facts

SNOMED CT: 711160007
UMLS CUI: C1850000
Fully Specified Name: Eosinophil peroxidase deficiency (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 1

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.