inborn metal metabolism disorder developmental anomaly of metabolic origin inherited renal tubular disease hereditary hypoparathyroidism pseudohypoparathyroidism https://rarediseases.info.nih.gov/diseases/10758/pseudohypoparathyroidism https://www.malacards.org/card/pseudohypoparathyroidism NANDO:1200776 Orphanet:97593 MONDO:0019992 ICD10CM:E20.1 MedDRA:10037126 NANDO:2100126 icd11.foundation:1225154856 NCIT:C99027 MEDGEN:46178 GARD:0010758 NORD:1627 ICD9:275.49 DOID:4184 UMLS:C0033806 Pseudohypoparathyroidism (PHP) is a heterogeneous group of endocrine disorders characterized by normal renal function and resistance to the action of parathyroid hormone (PTH), manifesting with hypocalcemia, hyperphosphatemia and elevated PTH levels and that includes the subtypes PHP type 1a (PHP-1a), PHP type 1b (PHP-1b), PHP type 1c (PHP-1c), PHP type 2 (PHP-2) and pseudopseudohypoparathyroidism (PPHP). NANDO:2200349 SCTID:58976002 MESH:D011547