MeSH Browser

MeSH Supplementary: Hypercalcemia, Idiopathic, of Infancy
Unique ID: C562581
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562581
Registry Numbers: 0
Heading Mapped to: *Hypercalcemia; *Infant, Newborn, Diseases; *Metabolism, Inborn Errors
Frequency: 22
Note: Severe hypercalcemia characterized by failure to thrive, vomiting, dehydration, and NEPHROCALCINOSIS. It is caused by mutations in the CYP24A1 gene. OMIM: 143880
Date of Entry: 2012/11/05
Revision Date: 2016/09/29

Hypercalcemia, Idiopathic, of Infancy MeSH Supplementary Concept Data 2025