Disease #01529 (LIDLS (Liddle syndrome (LIDLS)), OMIM:177200)

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Official abbreviation	LIDLS
Name	Liddle syndrome (LIDLS)
OMIM ID	177200
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 2 genes	SCNN1B, SCNN1G
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A