Cystic Fibrosis, also known as mucoviscidosis, is related to vas deferens, congenital bilateral aplasia of and bronchiectasis with or without elevated sweat chloride 1, and has symptoms including coughing, hemoptysis and snoring. An important gene associated with Cystic Fibrosis is CFTR (CF Transmembrane Conductance Regulator), and among its related pathways/superpathways are Embryonic and Induced Pluripotent Stem Cells and Lineage-specific Markers and Photodynamic therapy-induced NFE2L2 (NRF2) survival signaling. The drugs Ticarcillin and Clavulanic acid have been mentioned in the context of this disorder. Affiliated tissues include Lung and pancreas, and related phenotypes are recurrent respiratory infections and malabsorption