All diseases

OMIM ID
145980
OMIM term:
HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE I; HHC1
Alternative terms:
FHH1
FAMILIAL BENIGN HYPERCALCEMIA 1; FBH1
HYPERCALCEMIA, FAMILIAL BENIGN HYPOCALCIURIC HYPERCALCEMIA, ACQUIRED, INCLUDED
(∗) Location:
3q21.1  
(†) Associated OMIM genes:
CASR  
(‡) Associated MGI genes:
Casr  

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