Bartter Syndrome, Type 3, with Hypocalciuria MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Bartter Syndrome, Type 3, with Hypocalciuria
Unique ID: C564578
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564578
Registry Numbers: 0
Heading Mapped to: *Bartter Syndrome
Frequency: 0
Note: mutation in CLCNKB
Date of Entry: 2012/11/05
Revision Date: 2012/11/05

Bartter Syndrome, Type 3, with Hypocalciuria Preferred

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