Hereditary congenital prekallikrein deficiency

disorder

SNOMED 1162804003CUI C5566529

Overview

Hereditary congenital prekallikrein deficiency is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Related Conditions

Prekallikrein deficiency(parent)

Congenital disease(parent)

Recessive hereditary disorder (autosomal)(parent)

Quick Facts

SNOMED CT: 1162804003
UMLS CUI: C5566529
Fully Specified Name: Hereditary congenital prekallikrein 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.