Neonatal purpura fulminans due to homozygous protein C deficiency

disorder

SNOMED 402851000CUI C1274290

Overview

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

Related Conditions

Purpura fulminans(parent)

Homozygous protein C deficiency(parent)

Hereditary disorder of the integument(parent)

Cardiovascular system hereditary disorder(parent)

Purpura with coagulation disorder(parent)

Quick Facts

SNOMED CT: 402851000
UMLS CUI: C1274290
Fully Specified Name: Neonatal purpura fulminans due to homozygous protein C 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.