Liddle syndrome 1

MONDO:0020607

Any Liddle syndrome in which the cause of the disease is a mutation in the SCNN1B gene.

Also known as: Liddle syndrome 1, Liddle syndrome caused by mutation in SCNN1B, SCNN1B Liddle syndrome, LIDLS1, Liddle syndrome, Pseudoaldosteronism

11 clinical trials for this condition and its sub-types.

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