MeSH Browser

MeSH Supplementary: Hypercalciuric Hypocalcemia, Familial
Unique ID: C562783
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562783
Entry Term(s): Hypocalcemia, Autosomal Dominant; Hypocalcemia, Familial; Hypoparathyroidism, Autosomal Dominant
Registry Number: 0
Heading Mapped to: *Hypocalcemia; Hypoparathyroidism / *congenital; *Hypercalciuria
Frequency: 41
Note: PROM
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Hypercalciuric Hypocalcemia, Familial MeSH Supplementary Concept Data 2024