You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis, look for clinical trials, and connect with others living with it — all in one place.
Open the full Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis hub →Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis is a rare condition. Also known as FHHNC, Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis, Michellis-Castrillo syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:306516 · ICD-10 E83.4 · GARD 0021254
Start by learning the basics from an authoritative source, find a specialist or center that sees Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis, 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 primary hypomagnesemia with hypercalciuria and nephrocalcinosis, filtered to your area.
Tomeko shows live, recruiting studies for Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis from ClinicalTrials.gov on the hub.