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Hereditary angioedema type 3

Just diagnosed with Hereditary angioedema type 3?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Hereditary angioedema type 3, look for clinical trials, and connect with others living with it — all in one place.

Open the full Hereditary angioedema type 3 hub →

Overview

Hereditary angioedema type 3 is a rare condition. Also known as F12-related HAE with normal C1 inhibitor, HAE 3, HAE-III, Hereditary angioedema type 3, Hereditary angioneurotic edema type 3, Inherited estrogen-associated angioedema, Inherited estrogen-associated angioneurotic edema, Inherited estrogen-dependent angioedema. Tomeko brings together the specialists, research, clinical trials, treatments and community for Hereditary angioedema type 3 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:100054 · OMIM 610618 · ICD-10 T78.3 · GARD 0016935

Find care for Hereditary angioedema type 3

Authoritative references for Hereditary angioedema type 3

Common questions

I was just diagnosed with Hereditary angioedema type 3 — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Hereditary angioedema type 3, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Hereditary angioedema type 3?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Hereditary angioedema type 3, filtered to your area.

Are there clinical trials for Hereditary angioedema type 3?

Tomeko shows live, recruiting studies for Hereditary angioedema type 3 from ClinicalTrials.gov on the hub.

Informational only — not medical advice. Always consult a qualified clinician. Provider and reference data from public sources (NIH GARD, Orphanet, OMIM, HPO, MONDO, ClinicalTrials.gov, CMS NPPES). © Tomeko · tomekohealth.com