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familial hypocalciuric hypercalcemia 2 (DOID:0060701)
Synonyms: familial hypocalciuric hypercalcemia type 2; FHH type 2; HHC2; hypocalciuric hypercalcemia type II
Alt IDs: OMIM:145981, ICD10CM:E83.5, ORDO:101049
Definition: A familial hypocalciuric hypercalcemia that has_material_basis_in heterozygous mutation in the GNA11 gene on chromosome 19p13.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
05/23/2017
MGI 6.09
The Jackson Laboratory