Familial hypocalciuric hypercalcemia 3

MONDO:0010926

Any familial hypocalciuric hypercalcemia in which the cause of the disease is a mutation in the AP2S1 gene.

Also known as: AP2S1 familial hypocalciuric hypercalcemia, FHH type 3, HHC3, familial hypocalciuric hypercalcemia caused by mutation in AP2S1, familial hypocalciuric hypercalcemia type 3, hpocalciuric hypercalcemia, type III, FBH3, FBHOk

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