familial primary hypomagnesemia with normocalcuria
MONDO:0017626Mondo
Findings
No curated finding names familial primary hypomagnesemia with normocalcuria yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Familial primary hypomagnesemia with normocalcuria (FPHN) is a form of familial primary hypomagnesemia (FPH) which is characterized by low magnesium values but normal calcium values in the serum. The disorder consists of three distinct forms which are: autosomal recessive primary hypomagnesemia with normocalcuria and hypocalcemia (ARPHN), familial primary hypomagnesemia with normocalcuria and normocalcemia (FPHNN) and isolated autosomal dominant hypomagnesemia, Glaudemans type.
Definition from the Mondo Disease Ontology (MONDO:0017626), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of