Familial hypoparathyroidism

MONDO:0016390

A 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

12 clinical trials for this condition and its sub-types, 0 tagged with Familial hypoparathyroidism itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Inborn errors of metabolism (2228) ↑ Hereditary hypoparathyroidism (26)

Sub-types of Familial hypoparathyroidism

Autosomal dominant hypocalcemia 9 trials · 10 incl. sub-types
2 sub-types
- Autosomal dominant hypocalcemia 1 4 trials
- Autosomal dominant hypocalcemia 2 1 trial
Hypoparathyroidism, familial isolated 1 0 trials
2 sub-types
- Familial isolated hypoparathyroidism due to agenesis of parathyroid gland 0 trials
- Familial isolated hypoparathyroidism due to impaired PTH secretion 0 trials
Hypoparathyroidism, familial isolated, 2 0 trials

Including sub-types (12) Tagged with Familial hypoparathyroidism (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.