You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Congenital plasminogen activator inhibitor type 1 deficiency, look for clinical trials, and connect with others living with it — all in one place.
Open the full Congenital plasminogen activator inhibitor type 1 deficiency hub →Congenital plasminogen activator inhibitor type 1 deficiency is a rare condition. Also known as Congenital PAI-1 deficiency. Tomeko brings together the specialists, research, clinical trials, treatments and community for Congenital plasminogen activator inhibitor type 1 deficiency so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:465 · OMIM 613329 · ICD-10 D68.8 · GARD 0004381
Start by learning the basics from an authoritative source, find a specialist or center that sees Congenital plasminogen activator inhibitor type 1 deficiency, 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 Congenital plasminogen activator inhibitor type 1 deficiency, filtered to your area.
Tomeko shows live, recruiting studies for Congenital plasminogen activator inhibitor type 1 deficiency from ClinicalTrials.gov on the hub.