Familial hypoparathyroidism
MONDO:0016390A rare heterogeneous group of metabolic disorders characterized by abnormal calcium metabolism due to deficient secretion of parathormone (PTH), without other endocrine disorders or developmental defects.
Also known as: Familial Isolated Hypoparathyroidism, familial isolated hypoparathyroidism, hypoparathyroidism familial isolated, hypoparathyroidism, familial, hypoparathyroidism, familial isolated
11 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Autosomal dominant hypocalcemia
(8)
Autosomal dominant hypocalcemia 1
(4)
Autosomal dominant hypocalcemia 2
(1)
Familial isolated hypoparathyroidism due to agenesis of parathyroid gland
(0)
Familial isolated hypoparathyroidism due to impaired PTH secretion
(0)
Hypoparathyroidism, familial isolated 1
(0)
Hypoparathyroidism, familial isolated, 2
(0)