Autosomal dominant hypocalcemia 2

An autosomal dominant hypocalcemia disease that has material basis in heterozygous mutation in the GNA11 gene on chromosome 19p13.

Also known as: HYPOC2, autosomal dominant hypocalcemia type 2, hypocalcemia, autosomal dominant type 2, hypocalcemia, autosomal dominant 2

4 clinical trials for this condition and its sub-types, 1 tagged with Autosomal dominant hypocalcemia 2 itself.