Disease: LIDDLE SYNDROME 3 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4748292
Disease: LIDDLE SYNDROME 3
LIDDLE SYNDROME 3 		0.500 GeneticVariation disease UNIPROT A Missense Mutation in the Extracellular Domain of αENaC Causes Liddle Syndrome. 28710092 2017
CUI: C4748292
Disease: LIDDLE SYNDROME 3
LIDDLE SYNDROME 3 		0.500 Biomarker disease GENOMICS_ENGLAND Lung symptoms in pseudohypoaldosteronism type 1 are associated with deficiency of the alpha-subunit of the epithelial sodium channel. 10586178 1999