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Prothrombin G20210A mutation

disorder
SNOMED 440989002CUI C2584409

Overview

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

Related Conditions

Homozygous prothrombin G20210A mutation(child)
Heterozygous prothrombin G20210A mutation(child)
Hereditary thrombophilia(parent)
Autosomal dominant hereditary disorder(parent)

Quick Facts

SNOMED CT
440989002
UMLS CUI
C2584409
Fully Specified Name
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.