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

61 clinical trials for this condition and its sub-types, 0 tagged with Familial hypocalciuric hypercalcemia 3 itself.

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↑ Familial hypocalciuric hypercalcemia (1)

Including sub-types (61) Tagged with Familial hypocalciuric hypercalcemia 3 (0)

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