- OMIM ID
-
145981
- OMIM term:
- HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II; HHC2
- Alternative terms:
-
FAMILIAL BENIGN HYPERCALCEMIA, TYPE II; FBH2
HYPERCALCEMIA, FAMILIAL BENIGN, TYPE II
- (∗) Location:
- 19p13.3
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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