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hereditary angioedema type 1

MeSH: C538577ORPHA: 100050

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Clinical Presentation
  4. 4. Classification & Codes

Overview

Hereditary angioedema type 1 (HAE 1) is a form of hereditary angioedema (see this term) characterized by acute edema in subcutaneous tissues, viscera and/or the upper airway

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Clinical Presentation

Signs and symptoms associated with hereditary angioedema type 1, sourced from HPO and Orphanet clinical annotations.

Facial edemaUrticariaAbnormality of metabolism/homeostasisAbdominal painParesthesiaIntestinal edemaEdema of the dorsum of handsDermatographic urticariaLaryngeal edemaAbnormal respiratory system morphologyLimbal edemaTongue edemaVomitingDiarrheaDysphagiaNauseaDyspneaAbnormality of salivationAbnormal uvula morphologyHoarse voiceRespiratory distressHypotensionInspiratory stridorAbnormal epiglottis morphologyPharyngeal edemaAbnormal soft palate morphology

Classification & Codes

MeSH Code

C538577

Orphanet Code

ORPHA:100050
hereditary angioedema type 1
MeSHC538577
OrphanetORPHA:100050
Treatments0 drug(s)
Symptoms on record26 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO