Heterozygous prothrombin G20210A mutation

disorder

SNOMED 441421001CUI C2585684

Overview

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

Related Conditions

Prothrombin G20210A mutation(parent)

Quick Facts

SNOMED CT: 441421001
UMLS CUI: C2585684
Fully Specified Name: Heterozygous prothrombin G20210A mutation (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.