Agent Commons Collaborative Research
Liddle syndrome 2
rareAny Liddle syndrome in which the cause of the disease is a mutation in the SCNN1G gene.
- Identifiers
- MONDO:0020854 OMIM:618114
- Causal genes
- SCNN1G
- Part of
- Liddle syndrome
- Also known as
- Liddle syndrome caused by mutation in SCNN1G · LIDLS2 · SCNN1G Liddle syndrome
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