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Liddle Syndrome MeSH Descriptor Data 2023


MeSH Heading
Liddle Syndrome
Tree Number(s)
C12.050.351.968.419.815.683
C12.200.777.419.815.683
C12.950.419.815.683
C16.320.831.698
Unique ID
D056929
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D056929
Scope Note
Familial pseudoaldosteronism characterized by autosomal dominant inheritance of hypertension with HYPOKALEMIA; ALKALOSIS; RENIN and ALDOSTERONE level decreases. It is caused by mutations in EPITHELIAL SODIUM CHANNELS beta and gamma subunits. Different mutations in the same EPITHELIAL SODIUM CHANNELS subunits can cause PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT.
Entry Term(s)
Pseudoaldosteronism
See Also
Epithelial Sodium Channels
Public MeSH Note
2010
History Note
2010
Date Established
2010/01/01
Date of Entry
2009/07/06
Revision Date
2021/06/30
Liddle Syndrome Preferred
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