Homozygous protein S deficiency

disorder

SNOMED 441189007CUI C2586160

Overview

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

Related Conditions

Hereditary protein S deficiency(parent)

Quick Facts

SNOMED CT: 441189007
UMLS CUI: C2586160
Fully Specified Name: Homozygous protein S deficiency (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.