You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Familial juvenile hyperuricemic nephropathy type 2, look for clinical trials, and connect with others living with it — all in one place.
Open the full Familial juvenile hyperuricemic nephropathy type 2 hub →Familial juvenile hyperuricemic nephropathy type 2 is a rare condition. Also known as ADTKD-REN, FJHN type 2, Familial juvenile hyperuricemic nephropathy type 2, REN-associated FJHN, REN-associated familial juvenile hyperuricemic nephropathy, REN-associated kidney disease. Tomeko brings together the specialists, research, clinical trials, treatments and community for Familial juvenile hyperuricemic nephropathy type 2 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:217330 · OMIM 613092 · ICD-10 Q61.5 · GARD 0013461
Start by learning the basics from an authoritative source, find a specialist or center that sees Familial juvenile hyperuricemic nephropathy type 2, 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 Familial juvenile hyperuricemic nephropathy type 2, filtered to your area.
Tomeko shows live, recruiting studies for Familial juvenile hyperuricemic nephropathy type 2 from ClinicalTrials.gov on the hub.