Autosomal dominant hypocalcemia 1

MONDO:0011013

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

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

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