Familial hypocalciuric hypercalcemia 1

MONDO:0007791

Any familial hypocalciuric hypercalcemia in which the cause of the disease is a mutation in the CASR gene.

Also known as: CASR familial hypocalciuric hypercalcemia, FHH type 1, HHC1, familial benign hypercalcemia 1, familial hypocalciuric hypercalcemia caused by mutation in CASR, familial hypocalciuric hypercalcemia type 1, hpocalciuric hypercalcemia, type I, FBH1

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