Liddle syndrome

rare

A rare genetic form of low-renin hypertension characterized by hypertension associated with decreased plasma levels of potassium and aldosterone.

Identifiers: MONDO:0008323 Orphanet:526
Part of: Inherited kidney disorder Renal tubular transport disease Syndromic disease
Also known as: LIDLS · pseudoaldosteronism

Subtypes

Disease	ID	Genes
Liddle syndrome 1	MONDO:0020607	SCNN1B
Liddle syndrome 2	MONDO:0020854	SCNN1G
Liddle syndrome 3	MONDO:0029132

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