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

1469 clinical trials for this condition and its sub-types, 0 tagged with Hyperparathyroidism 4 itself.

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↑ Bone neoplasm (2118) ↑ Hereditary disorder of connective tissue (1314) ↑ Abnormal mineralization disorder (22) ↑ Familial isolated hyperparathyroidism (0)

Including sub-types (1469) Tagged with Hyperparathyroidism 4 (0)

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