Human genes for familial hypocalciuric hypercalcemia 2
Familial hypocalciuric hypercalcemia 2 [DOID:0060701]
A familial hypocalciuric hypercalcemia that has_material_basis_in heterozygous mutation in the GNA11 gene on chromosome 19p13.
Synonyms: familial hypocalciuric hypercalcemia 2, DOID:0060701, hereditary hypocalciuric hypercalcemia 2, familial hypocalciuric hypercalcemia type 2, FHH type 2 ...