← Back to Conditions

Myeloperoxidase deficiency

disorder
SNOMED 234433009CUI C0398595

Overview

Myeloperoxidase deficiency 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.

Diminished neutrophil myeloperoxidase activity
Always present (100%)HP:6000513
Hematologic disease
HP:0001871
Immunological abnormality
HP:0002715
Laboratory abnormality
HP:0001939
Reduced neutrophil myeloperoxidase activity
HP:6000375

Quick Facts

SNOMED CT
234433009
UMLS CUI
C0398595
Fully Specified Name
Myeloperoxidase deficiency (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
5
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.