Hereditary angioneurotic oedema with normal C1 esterase inhibitor activity

disorder

SNOMED 427167008CUI C1960459

Overview

Hereditary angioneurotic oedema with normal C1 esterase inhibitor activity is a disorder.

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

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Angiooedema

Very frequent (80-99%)HP:0100665

Edema of the upper limbs

Frequent (30-79%)HP:0010742

Facial swelling

Frequent (30-79%)HP:0000282

Intestinal edema

Frequent (30-79%)HP:0005225

Laryngeal edema

Frequent (30-79%)HP:0012027

Bleeding tendency

Occasional (5-29%)HP:0001892

Bronchial asthma

Occasional (5-29%)HP:0002099

Genital oedema

Occasional (5-29%)HP:0031188

Tongue oedema

Occasional (5-29%)HP:0040315

Upset stomach

Occasional (5-29%)HP:0002027

Tiredness

Very rare (1-4%)HP:0012378

Related Conditions

Autosomal dominant hereditary disorder(parent)

Hereditary angioneurotic edema(parent)

Quick Facts

SNOMED CT: 427167008
UMLS CUI: C1960459
Fully Specified Name: Hereditary angioedema with normal C1 esterase inhibitor activity (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 11

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.