Disease
Familial benign hypercalcemia
1 associated genes · 0 supporting PMIDs
Familial hypocalciuric hypercalcemia (FHH) is an inherited condition that can cause hypercalcemia, a serum calcium level typically above 10.2 mg/dL; although uncommon. It is also known as familial benign hypocalciuric hypercalcemia (FBHH) where there is usually a family history of hypercalcemia which is mild, a urine calcium to creatinine ratio <0.01, and urine calcium <200 mg/day (hypocalciuria).
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1 entryassociated with
| Gene | Score | PMIDs |
|---|---|---|
| CASR | 0.22 | 0 |