Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Bone neoplasm · Hereditary disorder of connective tissue · Abnormal mineralization disorder · Familial isolated hyperparathyroidism
Hyperparathyroidism 4
Any familial isolated hyperparathyroidism in which the cause of the disease is a mutation in the GCM2 gene.
This condition has no sub-types.