Disorder of GNAS inactivation
MONDO:0800466Any endocrine system disorder in which the cause of the disease is inactivation of the GNAS gene. Phenotypes include pseudohypoparathyroidism Ia, Ib, and Ic (PHP-Ia, -Ib, -Ic), pseudopseudohypoparathyroidism (PPHP), progressive osseous heteroplasia (POH), and osteoma cutis (OC).
7 clinical trials for this condition and its sub-types, 0 tagged with Disorder of GNAS inactivation itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Disorder of GNAS inactivation
-
Pseudohypoparathyroidism type 1A 7 trials
-
Pseudopseudohypoparathyroidism 2 trials
-
Progressive osseous heteroplasia 0 trials
-
Pseudohypoparathyroidism type 1B 0 trials
-
Pseudohypoparathyroidism type 1C 0 trials
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.