Autosomal dominant hypocalcemia 1

Any autosomal dominant hypocalcemia in which the cause of the disease is a mutation in the CASR gene.

Also known as: hypocalcemia, autosomal dominant, CASR autosomal dominant hypocalcemia, HYPOC1, autosomal dominant hypocalcemia caused by mutation in CASR, autosomal dominant hypocalcemia type 1, hypocalcemia, autosomal dominant type 1, hypocalcemia, autosomal dominant, with Bartter syndrome, hypercalciuric hypocalcemia

7 clinical trials for this condition and its sub-types.