Liddle syndrome 2
MONDO:0020854Any Liddle syndrome in which the cause of the disease is a mutation in the SCNN1G gene.
Also known as: LIDLS2, Liddle syndrome 2, Liddle syndrome caused by mutation in SCNN1G, SCNN1G Liddle syndrome
1 clinical trial for this condition and its sub-types, 0 tagged with Liddle syndrome 2 itself.
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