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
00129 BESC-1 bronchiectasis, with/without elevated sweat chloride, type 1, modifier of (BESC-1) 211400 - - - CFTR, SCNN1B - -
00131 CBAVD vas deferens, congenital bilateral absence (CBAVD) 277180 - - - CFTR - -
00128 CF cystic fibrosis (CF) 219700 - - - CFTR, FCGR2A, TGFB1 - -
00130 PCTT pancreatitis (PCTT) 167800 - - - CFTR, CTRC, PRSS1, SPINK1 - -
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