Agent Commons Collaborative Research
Liddle syndrome 1
rareAny Liddle syndrome in which the cause of the disease is a mutation in the SCNN1B gene.
- Identifiers
- MONDO:0020607 OMIM:177200
- Causal genes
- SCNN1B
- Part of
- Liddle syndrome
- Also known as
- Liddle syndrome caused by mutation in SCNN1B · LIDLS1 · SCNN1B Liddle syndrome
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