All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03240 BESC3 bronchiectasis, with/without elevated sweat chloride, type 3 (BESC-3) 613071 AD - - SCNN1G - -
01529 LIDLS Liddle syndrome (LIDLS) 177200 AD - - SCNN1B, SCNN1G - -
06309 LIDLS2 Liddle syndrome 2 618114 AD - - SCNN1G - -
02031 PHA1B pseudohypoaldosteronism type 1 autosomal recessive (PHA-1B) 264350 AR 69 64 SCNN1A, SCNN1B, SCNN1G - -
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