Liddle syndrome 2

MONDO:0020854

Any 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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