Any familial hypocalciuric hypercalcemia in which the cause of the disease is a mutation in the CASR gene.
Comprehensive, easy-to-understand information about this condition
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chondrocalcinosis 2
MONDO:0007319
hyperparathyroidism 1
MONDO:0007767
hyperparathyroidism 2 with jaw tumors
MONDO:0007768
familial hypocalciuric hypercalcemia 2
MONDO:0007792
autosomal dominant hypophosphatemic rickets
MONDO:0008660
neonatal severe primary hyperparathyroidism
MONDO:0009397