Keyphrases
Cystic Fibrosis
100%
Clinical Phenotyping
100%
National Cohort
100%
Cystic Fibrosis Foundation
33%
Disease Manifestations
33%
Cystic Fibrosis Transmembrane Conductance Regulator
33%
Lung Function
16%
Diabetes
16%
Clinical Data
16%
Genetic Variation
16%
High Risk
16%
Genotype
16%
Environmental Factors
16%
Patient Registry
16%
Statistical Learning
16%
Genetic Factors
16%
Minimal Function
16%
Pretransplant
16%
Medical Complexity
16%
High Prevalence
16%
Cholestatic Liver Disease
16%
Adult Age
16%
Spirometry
16%
Highly Similar
16%
Multisystem Disease
16%
Clinical Phenotype
16%
Chronic Sinusitis
16%
Aides
16%
Physiological Parameters
16%
Bronchiectasis
16%
Random Forest
16%
Clustering Algorithm
16%
Demographic Parameters
16%
Robust Techniques
16%
Malabsorption
16%
P. Aeruginosa Infection
16%
Well-nourished
16%
Pancreatic Insufficiency
16%
Nutritional Characteristics
16%
Male-dominated
16%
Risk Phenotypes
16%
Older Survivors
16%
Pseudomonas Aeruginosa Colonization
16%
Distal Intestinal Obstruction Syndrome
16%
Partitioning around Medoids
16%
Medicine and Dentistry
Cystic Fibrosis
100%
Pseudomonas aeruginosa
33%
Cystic Fibrosis Transmembrane Conductance Regulator
33%
Diseases
33%
Lung
16%
Infection
16%
Diabetes
16%
Regulator Gene
16%
Prevalence
16%
Patient Registry
16%
Systemic Disease
16%
Liver Disease
16%
Spirometry
16%
Environmental Factor
16%
Bronchiectasis
16%
Genetic Variation
16%
Malabsorption
16%
Chronic Sinusitis
16%
Pancreatic Insufficiency
16%
Nutritive Value
16%
Biochemistry, Genetics and Molecular Biology
Cystic Fibrosis
100%
Pseudomonas aeruginosa
33%
Cystic Fibrosis Transmembrane Conductance Regulator
33%
Genetics
16%
Genetic Divergence
16%
Locus Control Region
16%
Patient Registry
16%
Genetic Variation
16%
Prevalence
16%
Random Forest
16%