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Hypercalcemia, Infantile [Supplementary Concept]

Severe hypercalcemia that occurs in infancy and is characterized by elevated calcium levels in blood and urine, failure to thrive, vomiting , dehydration, and NEPHROCALCINOSIS. HCINF1 is caused by mutations in the CYP24A1 gene (OMIM: 143880) and HCINF2 is caused by mutations in the SLC34A1 gene (OMIM: 616963).

Date introduced: November 5, 2012

MeSH Unique ID: C562999

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Entry Terms:

  • Hypercalcemia, Infantile, 1
  • Hypercalcemia, infantile, 2

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