disease has basis in dysfunction of disease has feature GNAS Short stature pseudohypoparathyroidism type 1A AHO AHO-PHP syndrome Ia Albright hereditary osteodystrophy Albright hereditary osteodystrophy with multiple hormone resistance Albright hereditary osteodystrophy-PHP syndrome Ia Albright's hereditary osteodystrophy DOID:0080053 GARD:0005770 GARD:0007486 ICD10:E20.1 ICD9:275.49 MESH:C537045 MONDO:0007078 NCIT:C129721 OMIM:103580 Orphanet:79443 PHP 1A PHP1A Pseudohypoparathyroidism type 1A (PHP1a) is a type of pseudohypoparathyroidism (PHP) characterized by renal resistance to parathyroid hormone (PTH), resulting in hypocalcemia, hyperphosphatemia, and elevated PTH; resistance to other hormones including thydroid stimulating hormone (TSH), gonadotropins and growth-hormone-releasing hormone (GHRH); and a constellation of clinical features known as Albright hereditary osteodystrophy (AHO). SCTID:58833000 UMLS:C2931404 UMLS:C3494506 pseudohypoparathyroidism type 1A pseudohypoparathyroidism, type 1A pseudohypoparathyroidism, type IA syndromic genetic obesity other genetic dermis disorder acromelic dysplasia pseudohypoparathyroidism musculoskeletal disease with cataract dermis disease hereditary connective tissue disorder genetic skin disease