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Summary Literature (0)
DOID:0060699 - familial hypocalciuric hypercalcemia

Disease Ontology Definition:A hypercalcemia characterized by autosomal dominant inheritance with elevation of serum calcium levels and decreased urinary calcium excretion.

Synonyms: familial benign hypercalcemia, familial benign hypocalciuric hypercalcemia, FBH, FBHH, FHH

Xenbase Genes : gna11, ap2s1, casr

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0018458 - familial hypocalciuric hypercalcemia


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), hypercalcemia (is_a), inherited metabolic disorder (is_a)