Familial benign hypercalcemia Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Familial hypocalciuric hypercalcemia (FHH) is a generally asymptomatic genetic disorder of phosphocalcic metabolism characterized by lifelong moderate hypercalcemia along with normo- or hypocalciuria and elevated plasma parathyroid hormone (PTH) concentration. (Orphanet Rare Disease Ontology, Orphanet_405)
External Link http://www.omim.org/entry/145980
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Genes

1 genes associated with the Familial benign hypercalcemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
CASR calcium-sensing receptor