familial hypocalciuric hypercalcemia Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
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Genes

1 genes associated with the disease familial hypocalciuric hypercalcemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
CASR calcium-sensing receptor