MeSH Browser

MeSH Supplementary: Hypokalemia, Familial
Unique ID: C562654
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562654
Entry Term(s): Gullner Syndrome; Hypokalemic Alkalosis, Familial, with Specific Renal Tubulopathy
Heading Mapped to: *Hypokalemia; *Metabolism, Inborn Errors
Frequency: 2
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Hypokalemia, Familial MeSH Supplementary Concept Data 2024