Autosomal dominant hypocalcemia 2

MONDO:0014146

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

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

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