Renal hypomagnesemia 3

MONDO:0009550

Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (FHHN) is a form of familial primary hypomagnesemia (FPH), characterized by recurrent urinary tract infections, nephrolithiasis, bilateral nephrocalcinosis, renal magnesium (Mg) wasting, hypercalciuria and kidney failure.

Also known as: CLDN16 familial primary hypomagnesemia, CLDN16 primary hypomagnesemia, FHHNC without severe ocular involvement, HOMG3, familial primary hypomagnesemia caused by mutation in CLDN16, primary hypomagnesemia caused by mutation in CLDN16, renal hypomagnesemia type 3, hypercalciuria, childhood, self-limiting

35 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by