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

Gå till den engelska sidan

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

62 clinical trials for this condition and its sub-types, 1 tagged with Familial hypocalciuric hypercalcemia 1 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by