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Familial hypocalciuric hypercalcemia
rareFamilial 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.
- Identifiers
- MONDO:0018458 Orphanet:405
- Part of
- Endocrine system disorderHypercalcemia diseaseInborn errors of metabolismInherited interstitial lung diseaseInterstitial lung disease specific to childhood
- Also known as
- familial benign hypercalcemia · familial benign hypocalciuric hypercalcemia · FBH · FBHH · FHH
Subtypes
Rare disease
Projects
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