Any Liddle syndrome in which the cause of the disease is a mutation in the SCNN1G gene. [ MONDO:patterns/disease_series_by_gene ]
Synonyms: LIDLS2 Liddle syndrome caused by mutation in SCNN1G Liddle syndrome 2 SCNN1G Liddle syndrome
Term information
- OMIM:618114 (MONDO:equivalentTo)
- MEDGEN:1648476 (MONDO:equivalentTo)
- UMLS:C4748251 (MONDO:equivalentTo)
gard_rare, otar, rare
http://identifiers.org/medgen/1648476
https://omim.org/entry/618114
http://linkedlifedata.com/resource/umls/id/C4748251