Hyperaldosteronism, Familial, Type II MeSH Supplementary Concept Data 2025

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MeSH Supplementary: Hyperaldosteronism, Familial, Type II
Unique ID: C565312
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565312
Registry Numbers: 0
Heading Mapped to: *Hyperaldosteronism
Frequency: 3
Date of Entry: 2012/11/05
Revision Date: 2012/11/05

Hyperaldosteronism, Familial, Type II Preferred

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