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Disease Ontology Browser
familial hypocalciuric hypercalcemia (DOID:0060699)
Alliance: disease page
Synonyms: familial benign hypercalcemia; familial benign hypocalciuric hypercalcemia; FBH; FBHH; FHH
Alt IDs: ICD10CM:E83.5, OMIM:PS145980, ORDO:405
Definition: A hypercalcemia characterized by autosomal dominant inheritance with elevation of serum calcium levels and decreased urinary calcium excretion.

Disease References using Mouse Models (2)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory