Disorders with generalized decrease in sensitivity to Ca2+ (affecting all CaSR-expressing tissue) |
FHH |
NHPT and NSHPT |
Familial isolated hyperparathyroidism caused by CaSR mutations |
Autoimmune hypocalciuric hypercalcemia |
Disorders with parathyroid-specific decrease in sensitivity to Ca2+ |
Primary hyperparathyroidism |
Severe uremic secondary and tertiary hyperparathyroidism |
Disorders with generalized increase in sensitivity to Ca2+ |
ADH due to activating CaSR mutations |
ADH with features of Bartter syndrome |
Hypoparathyroidism due to activating antibodies to the CaSR |
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