A>gamma< beta^+^ HPFH AND beta^0^ thalassemia in cis

disorder

SNOMED 5967006CUI C0271989

Overview

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

Related Conditions

HPFH A gamma beta^+^ thalassemia(parent)

Quick Facts

SNOMED CT: 5967006
UMLS CUI: C0271989
Fully Specified Name: A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis (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.