A disease characterized by a constellation of clinical features collectively termed Albright hereditary osteodystrophy (AHO) but no evidence of resistance to parathyroid hormone (PTH), which is seen in other forms of pseudohypoparathyroidism (PHP). The disease is MONDO_0012912 (pseudopseudohypoparathyroidism). Also known as: Albright Hereditary osteodystrophy with multiple hormone resistance, Albright hereditary osteodystrophy-PPHP syndrome, Normocalcemic pseudohypoparathyroidism, Normocalcemic pseudohypoparathyroidism (disorder) [ambiguous], aho-PPHP syndrome.