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Familial hypocalciuric hypercalcemia 1
rareAny familial hypocalciuric hypercalcemia in which the cause of the disease is a mutation in the CASR gene.
- Identifiers
- MONDO:0007791 OMIM:145980Orphanet:93372
- Causal genes
- CASR
- Also known as
- CASR familial hypocalciuric hypercalcemia · familial benign hypercalcemia 1 · familial benign hypercalcemia type 1 · familial hypocalciuric hypercalcemia caused by mutation in CASR · familial hypocalciuric hypercalcemia type 1
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