Hereditary angioneurotic edema - type 2

disorder

SNOMED 234620006CUI C0398776

Overview

Hereditary angioneurotic edema - type 2 is a disorder.

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

Related Conditions

Hereditary disorder of immune system(parent)

Complement regulatory factor defect(parent)

Autosomal dominant hereditary disorder(parent)

Angioedema due to disorder of kinin metabolism(parent)

Hereditary angioedema with C1Inh (C1 esterase inhibitor) deficiency(parent)

Quick Facts

SNOMED CT: 234620006
UMLS CUI: C0398776
Fully Specified Name: Hereditary C1 esterase inhibitor deficiency - dysfunctional factor (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.