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Summary Literature (0)
DOID:0060701 - familial hypocalciuric hypercalcemia 2

Disease Ontology Definition:A familial hypocalciuric hypercalcemia that has_material_basis_in heterozygous mutation in the GNA11 gene on chromosome 19p13.

Synonyms: familial hypocalciuric hypercalcemia type 2, FHH type 2, HHC2, hypocalciuric hypercalcemia type II

Xenbase Genes : gna11

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007792 - familial hypocalciuric hypercalcemia 2

MIM:
MIM:145981 - HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II; HHC2

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): familial hypocalciuric hypercalcemia (is_a)