Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

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.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by