All diseases

OMIM ID
600740
OMIM term:
HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III; HHC3
Alternative terms:
FAMILIAL BENIGN HYPERCALCEMIA, TYPE III; FBH3
HYPERCALCEMIA, FAMILIAL BENIGN, TYPE III
HYPERCALCEMIA, FAMILIAL BENIGN, OKLAHOMA TYPE
(∗) Location:
19q13  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/mzcvc1m4