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Hereditary C1 Esterase Inhibitor Deficiency Dysfunctional Factor C0398776

Published: July 22, 2026Updated: August 20, 2026

Hereditary angioedema caused by a C1 inhibitor protein that is present but does not work properly. Leads to recurrent episodes of swelling in various body parts. Managed with specific therapies and preventive measures.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 20, 2026Editorial policy

Key facts at a glance

ICD-10
R69
ICD-11
MA00.0
Body system
immunologic
Severity
moderate
Chronic
true

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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy