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