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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: FBH, FBHH, FHH, familial benign hypercalcemia, familial benign hypocalciuric hypercalcemia,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
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)