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Familial hypocalciuric hypercalcemia 2
MONDO:0007792A familial hypocalciuric hypercalcemia that has material basis in heterozygous mutation in the GNA11 gene on chromosome 19p13.
Also known as: FHH type 2, HHC2, familial hypocalciuric hypercalcemia type 2, hpocalciuric hypercalcemia, type II, FBH2, familial benign hypercalcemia, type 2, hypercalcemia, familial benign type 2, hypercalcemia, familial benign, type 2
61 clinical trials for this condition and its sub-types, 0 tagged with Familial hypocalciuric hypercalcemia 2 itself.
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