MeSH Browser

MeSH Supplementary: Manz syndrome
Unique ID: C535709
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535709
Entry Term(s): Familial hypomagnesemia - hypercalciuria
Registry Number: 0
Heading Mapped to: *Magnesium Deficiency; *Nephrocalcinosis
Frequency: 11
Note: Polyuria, nystagmus and recurrent episodes of tetany with radiological evidence of rickets and nephrocalcinosis
Date of Entry: 2010/08/25

Manz syndrome MeSH Supplementary Concept Data 2024