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Hyperparathyroidism 4

MONDO:0024570

Any familial isolated hyperparathyroidism in which the cause of the disease is a mutation in the GCM2 gene.

Also known as: GCM2 familial isolated hyperparathyroidism, familial isolated hyperparathyroidism caused by mutation in GCM2, hyperparathyroidism 4, hyperparathyroidism type 4, HRPT4

1463 clinical trials for this condition and its sub-types, 0 tagged with Hyperparathyroidism 4 itself.

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Showing the 400 most recently updated of 713 trials in this tab.