Liddle syndrome 1
MONDO:0020607Any 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
1 clinical trial for this condition and its sub-types, 0 tagged with Liddle syndrome 1 itself.
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