Familial isolated hyperparathyroidism

rare

A rare, autosomal dominant hereditary syndrome characterized by hypercalcemia, abnormally high levels of parathyroid hormone, and isolated hyperfunctioning parathyroid tumors.

Identifiers: MONDO:0015027 Orphanet:99879
Part of: Familial primary hyperparathyroidism Hereditary neoplastic syndrome
Also known as: FIHP · FIHPT

Subtypes

All diseases Rare only

Disease

Hyperparathyroidism 1 MONDO:0007767 CDC73
Hyperparathyroidism 3 MONDO:0012406
Hyperparathyroidism 4 MONDO:0024570 GCM2

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