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Hereditary pyropoikilocytosis

disorder
SNOMED 9434008CUI C0520739

Overview

Hereditary pyropoikilocytosis 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.

Hemolytic anaemia
HP:0001878
Hereditary elliptocytosis
HP:0004445
Microspherocytosis
HP:0004835
Pyropoikilocytosis
HP:0004839

Quick Facts

SNOMED CT
9434008
UMLS CUI
C0520739
Fully Specified Name
Hereditary pyropoikilocytosis (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
4
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.