Hereditary elliptocytosis due to beta spectrin defect in self-association

disorder

SNOMED 73073009CUI C0272041

Overview

Hereditary elliptocytosis due to beta spectrin defect in self-association is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Related Conditions

Autosomal dominant hereditary disorder(parent)

Hereditary ovalocytosis(parent)

Quick Facts

SNOMED CT: 73073009
UMLS CUI: C0272041
Fully Specified Name: Hereditary elliptocytosis due to beta spectrin defect in self-association (disorder)
Specialists: 0
Diagnostic Biomarkers: 0

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.

Hereditary elliptocytosis due to beta spectrin defect in self-association — Symptoms, Testing & Specialists | Ltrl | Healos