Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Developmental anomaly of metabolic origin · Inborn metal metabolism disorder · Inherited renal tubular disease · Hereditary hypoparathyroidism
Pseudohypoparathyroidism
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).
-
Pseudohypoparathyroidism type 1A 7 trials
-
Pseudopseudohypoparathyroidism 2 trials
-
Pseudohypoparathyroidism type 1B 0 trials
-
Pseudohypoparathyroidism type 1C 0 trials
-
Pseudohypoparathyroidism type 2 0 trials