You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Autosomal dominant pseudohypoaldosteronism type 1, look for clinical trials, and connect with others living with it — all in one place.
Open the full Autosomal dominant pseudohypoaldosteronism type 1 hub →Autosomal dominant pseudohypoaldosteronism type 1 is a rare condition. Also known as Autosomal dominant PHA1, Autosomal dominant pseudohypoaldosteronism type 1, Renal PHA1. Tomeko brings together the specialists, research, clinical trials, treatments and community for Autosomal dominant pseudohypoaldosteronism type 1 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:171871 · OMIM 177735 · ICD-10 N25.8 · GARD 0009145
Start by learning the basics from an authoritative source, find a specialist or center that sees Autosomal dominant pseudohypoaldosteronism type 1, 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 Autosomal dominant pseudohypoaldosteronism type 1, filtered to your area.
Tomeko shows live, recruiting studies for Autosomal dominant pseudohypoaldosteronism type 1 from ClinicalTrials.gov on the hub.