Non-histaminic angioedema

disease
On this page

Also known as angioneurotic edemaangioneurotic oedemabradykinine-induced angioedemanon histamine-induced angioedema

Summary

Non-histaminic angioedema (MONDO:0019013) is a disease and 4 clinical trials. Top therapeutic interventions include conestat alfa and icatibant. A subtype of allergic urticaria — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Prevalence: 1-9 / 100 000 (Europe)
  • Clinical trials: 4

Clinical features

Epidemiology

Prevalence records

1 prevalence record(s), Orphanet:

TypeClassValueGeographyValidation
Point prevalence1-9 / 100 000EuropeNot yet validated

Identifiers

Disease identifiers

FieldValue
Canonical namenon-histaminic angioedema
Mondo IDMONDO:0019013
Orphanet658
SNOMED CT41291007
GARD0018701
Is cancer (heuristic)no

Also known as: angioneurotic edema · angioneurotic oedema · bradykinine-induced angioedema · non histamine-induced angioedema

Disease family

This is a subtype of allergic urticaria. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by body system or component › integumentary system disorder › skin disorderdermatitisatopic eczemaallergic urticarianon-histaminic angioedema

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 4.

Phase distribution (across all retrieved trials)

PhaseTrials
PHASE2/PHASE31
PHASE31
PHASE21
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00225147PHASE2/PHASE3COMPLETEDRecombinant Human C1 Inhibitor for the Treatment of Acute Attacks in Patients With Hereditary Angioedema
NCT00262301PHASE3COMPLETEDRecombinant Human C1 Inhibitor for the Treatment of Acute Attacks in Patients With Hereditary Angioedema
NCT00119431PHASE2COMPLETEDKinetics, Efficacy and Safety of C1-Esteraseremmer-N
NCT00517582PHASE1TERMINATEDBradykinin Receptor Blocker in ACE Inhibitor-associated Angioedema

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
CONESTAT ALFA42
ICATIBANT42