Familial hypocalciuric hypercalcemia

MONDO:0018458

Familial hypocalciuric hypercalcemia (FHH) is a generally asymptomatic genetic disorder of phosphocalcic metabolism characterized by lifelong moderate hypercalcemia along with normo- or hypocalciuria and elevated plasma parathyroid hormone (PTH) concentration.

Also known as: familial benign hypercalcemia, familial benign hypocalciuric hypercalcemia, FBH, FBHH, FHH, hypocalciuric hypercalcemia

62 clinical trials for this condition and its sub-types, 0 tagged with Familial hypocalciuric hypercalcemia itself.

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Where it sits in the disease tree

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↑ Endocrine system disorder (12469) ↑ Inborn errors of metabolism (2228) ↑ Interstitial lung disease specific to childhood (163) ↑ Inherited interstitial lung disease (11) ↑ Hypercalcemia disease (7)

Sub-types of Familial hypocalciuric hypercalcemia

Familial hypocalciuric hypercalcemia 1 1 trial
Familial hypocalciuric hypercalcemia 2 0 trials
Familial hypocalciuric hypercalcemia 3 0 trials

Including sub-types (62) Tagged with Familial hypocalciuric hypercalcemia (0)

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