Monarch Disease Ontology id MONDO_0011013 (autosomal dominant hypocalcemia 1) is any autosomal dominant hypocalcemia in which the cause of the disease is a mutation in the CASR gene. Also known as: 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.