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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease hyperparathyroidism
Comorbidity C0342637|familial hypocalciuric hypercalcaemia
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PubMedID- 23081733 Primary hyperparathyroidism in a patient with familial hypocalciuric hypercalcaemia due to a novel mutation in the calcium-sensing receptor gene.

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