Pseudohypoparathyroidism type 1C

MONDO:0012911

A rare type of pseudohypoparathyroidism (PHP) characterized by resistance to parathyroid hormone (PTH) and other hormones, which manifests with hypocalcemia, hyperphosphatemia and elevated PTH levels, a constellation of clinical features collectively termed Albright's hereditary osteodystrophy (AHO), but normal activity of the stimulatory protein G (Gs alpha).

Also known as: pseudohypoparathyroidism Ic, PHP1C, Php 1C, pseudohypoparathyroidism, type 1C, pseudohypoparathyroidism, type IC

3 clinical trials for this condition and its sub-types, 0 tagged with Pseudohypoparathyroidism type 1C itself.

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↑ Osteonecrosis of genetic origin (102) ↑ Primary avascular necrosis (39) ↑ Pseudohypoparathyroidism (9) ↑ Acromelic dysplasia (8) ↑ Disorder of GNAS inactivation (7)

Including sub-types (3) Tagged with Pseudohypoparathyroidism type 1C (0)

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