Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia

disorder

SNOMED 61395005CUI C0271999

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Related Conditions

Hereditary persistence of fetal hemoglobin thalassemia(parent)

Beta plus thalassemia(parent)

Quick Facts

SNOMED CT: 61395005
UMLS CUI: C0271999
Fully Specified Name: Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia (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.