You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Pseudohypoaldosteronism, type IB1, autosomal recessive, look for clinical trials, and connect with others living with it — all in one place.
Open the full Pseudohypoaldosteronism, type IB1, autosomal recessive hub →Pseudohypoaldosteronism, type IB1, autosomal recessive is a rare condition. Also known as Autosomal recessive PHA1, Autosomal recessive pseudohypoaldosteronism type 1, Generalized PHA1. Tomeko brings together the specialists, research, clinical trials, treatments and community for Pseudohypoaldosteronism, type IB1, autosomal recessive so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:171876 · OMIM 264350, 620125, 620126 · ICD-10 N25.8 · GARD 0004552
Start by learning the basics from an authoritative source, find a specialist or center that sees Pseudohypoaldosteronism, type IB1, autosomal recessive, 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 Pseudohypoaldosteronism, type IB1, autosomal recessive, filtered to your area.
Tomeko shows live, recruiting studies for Pseudohypoaldosteronism, type IB1, autosomal recessive from ClinicalTrials.gov on the hub.