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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: FHH type 2, HHC2, familial hypocalciuric hypercalcemia type 2, hypocalciuric hypercalcemia type II,
Echinobase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
familial hypocalciuric hypercalcemia (is_a)