Cystic Fibrosis (CF)

Cystic Fibrosis(来自ICD-11)

别称:

Mucoviscidosis

Pseudomonas Aeruginosa, Susceptibility to Chronic Infection by, in Cystic Fibrosis

Pseudomonas Aeruginosa Chronic Infection by, in Cystic Fibrosis

Cystic Fibrosis Lung Disease, Modifier of

Nonproliferative Fibrocystic Disease

Fibrocystic Disease of the Pancreas

Fibrocystic Disease of Pancreas

Cystic Fibrosis of Pancreas

Mucoviscidosis of Pancreas

Pancreatic Cystic Fibrosis

Cf - [cystic Fibrosis]

Cystic Fibrosis Nos

Fibrocystic Disease

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

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

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