Conditions / Genetic

familial hypocalciuric hypercalcemia

info · Genetic · ICD-10: E83.5

A hypercalcemia characterized by autosomal dominant inheritance with elevation of serum calcium levels and decreased urinary calcium excretion.

Also known as: FBH; FBHH; FHH; familial benign hypercalcemia; familial benign hypocalciuric hypercalcemia