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Familial hypocalciuric hypercalcemia 2
rareA familial hypocalciuric hypercalcemia that has material basis in heterozygous mutation in the GNA11 gene on chromosome 19p13.
- Identifiers
- MONDO:0007792 OMIM:145981Orphanet:101049
- Causal genes
- GNA11
- Also known as
- familial hypocalciuric hypercalcemia type 2 · FBH2 · FHH type 2 · HHC2 · hpocalciuric hypercalcemia, type II
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