Homozygous prothrombin G20210A mutation

disorder

SNOMED 441420000CUI C2586176

Overview

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

Related Conditions

Prothrombin G20210A mutation(parent)

Quick Facts

SNOMED CT: 441420000
UMLS CUI: C2586176
Fully Specified Name: Homozygous 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.