RS28936684 CASR
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What This Variant Does
"[OMIM:HYPERPARATHYROIDISM, NEONATAL SEVERE PRIMARY]
Associated Conditions
Neonatal severe primary hyperparathyroidism
Autosomal dominant hypocalcemia 1
Familial hypocalciuric hypercalcemia
CASR-related disorder
Familial hypocalciuric hypercalcemia 1
Familial hypocalciuric hypercalcemia
Autosomal dominant hypocalcemia 1
Epilepsy
idiopathic generalized
susceptibility to
8
Neonatal severe primary hyperparathyroidism
CASR-related disorder
Nephrolithiasis/nephrocalcinosis
Neonatal severe primary hyperparathyroidism
Other Variants in CASR