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 →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
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.
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Hereditary angioedema type 3, filtered to your area.
Tomeko shows live, recruiting studies for Hereditary angioedema type 3 from ClinicalTrials.gov on the hub.