disease has basis in dysfunction of GNAS pseudopseudohypoparathyroidism Albright Hereditary osteodystrophy with Multiple hormone Resistance Albright hereditary osteodystrophy without multiple hormone resistance Albright hereditary osteodystrophy-PPHP syndrome DOID:4183 GARD:0007860 ICD10:E20.1 ICD9:275.49 MESH:D011556 MONDO:0012912 NCIT:C129722 Normocalcemic pseudohypoparathyroidism Normocalcemic pseudohypoparathyroidism (disorder) [ambiguous] OMIM:612463 Orphanet:665 Orphanet:79445 PPHP Pseudopseudo-hypoparathyroidism Pseudopseudohypoparathyroidism (pseudo-PHP) is 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). SCTID:237659007 UMLS:C0033835 aho-PPHP syndrome https://rarediseases.info.nih.gov/diseases/7860/pseudopseudohypoparathyroidism pseudo-pseudohypoparathyroidism pseudopseudohypoparathyroidism syndromic genetic obesity other genetic dermis disorder acromelic dysplasia pseudohypoparathyroidism musculoskeletal disease with cataract dermis disease hereditary connective tissue disorder genetic skin disease