All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00129 BESC-1 bronchiectasis, with/without elevated sweat chloride, type 1, modifier of (BESC-1) 211400 - - - CFTR, SCNN1B - -
01529 LIDLS Liddle syndrome (LIDLS) 177200 - - - SCNN1B, SCNN1G - -
02031 PHA-1B pseudohypoaldosteronism type 1 autosomal recessive (PHA-1B) 264350 - - - SCNN1A, SCNN1B, SCNN1G - -
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