Turner's phenotype, partial X deletion karyotype

disorder

SNOMED 254280007CUI C0432459

Overview

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

Related Conditions

Turner syndrome(parent)

Quick Facts

SNOMED CT: 254280007
UMLS CUI: C0432459
Fully Specified Name: Turner's phenotype, partial X deletion karyotype (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.