Condition | Indicated | Relationship Strength | Studies | Trials |
Cryptogenic Fibrosing Alveolitis [description not available] | 0 | 3.47 | 6 | 0 |
Idiopathic Pulmonary Fibrosis A common interstitial lung disease of unknown etiology, usually occurring between 50-70 years of age. Clinically, it is characterized by an insidious onset of breathlessness with exertion and a nonproductive cough, leading to progressive DYSPNEA. Pathological features show scant interstitial inflammation, patchy collagen fibrosis, prominent fibroblast proliferation foci, and microscopic honeycomb change. | 0 | 3.47 | 6 | 0 |
Carcinoma, Non-Small Cell Lung [description not available] | 0 | 2.66 | 2 | 0 |
Cancer of Lung [description not available] | 0 | 2.66 | 2 | 0 |
Carcinoma, Non-Small-Cell Lung A heterogeneous aggregate of at least three distinct histological types of lung cancer, including SQUAMOUS CELL CARCINOMA; ADENOCARCINOMA; and LARGE CELL CARCINOMA. They are dealt with collectively because of their shared treatment strategy. | 0 | 2.66 | 2 | 0 |
Lung Neoplasms Tumors or cancer of the LUNG. | 0 | 2.66 | 2 | 0 |
Facial Palsy [description not available] | 0 | 2.41 | 1 | 0 |
Cardiac Failure [description not available] | 0 | 3.33 | 1 | 0 |
Pulmonary Hypertension [description not available] | 0 | 3.57 | 2 | 0 |
Heart Failure A heterogeneous condition in which the heart is unable to pump out sufficient blood to meet the metabolic need of the body. Heart failure can be caused by structural defects, functional abnormalities (VENTRICULAR DYSFUNCTION), or a sudden overload beyond its capacity. Chronic heart failure is more common than acute heart failure which results from sudden insult to cardiac function, such as MYOCARDIAL INFARCTION. | 0 | 3.33 | 1 | 0 |
Hypertension, Pulmonary Increased VASCULAR RESISTANCE in the PULMONARY CIRCULATION, usually secondary to HEART DISEASES or LUNG DISEASES. | 0 | 3.57 | 2 | 0 |
2019 Novel Coronavirus Disease [description not available] | 0 | 3.95 | 3 | 0 |
Breathlessness [description not available] | 0 | 3.68 | 2 | 0 |
chronic COVID syndrome [description not available] | 0 | 3.33 | 1 | 0 |
Dyspnea Difficult or labored breathing. | 0 | 3.68 | 2 | 0 |
Atrial Septal Defect [description not available] | 0 | 2.41 | 1 | 0 |
Airflow Obstruction, Chronic [description not available] | 0 | 4.11 | 12 | 0 |
Cystic Fibrosis of Pancreas [description not available] | 0 | 6.01 | 8 | 0 |
Cystic Fibrosis An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION. | 0 | 6.01 | 8 | 0 |
Pulmonary Disease, Chronic Obstructive A disease of chronic diffuse irreversible airflow obstruction. Subcategories of COPD include CHRONIC BRONCHITIS and PULMONARY EMPHYSEMA. | 0 | 4.11 | 12 | 0 |
Centriacinar Emphysema [description not available] | 0 | 2.98 | 3 | 0 |
Emphysema A pathological accumulation of air in tissues or organs. | 0 | 2.94 | 3 | 0 |
Benign Neoplasms [description not available] | 0 | 2.25 | 1 | 0 |
Neoplasms New abnormal growth of tissue. Malignant neoplasms show a greater degree of anaplasia and have the properties of invasion and metastasis, compared to benign neoplasms. | 0 | 2.25 | 1 | 0 |
Asthma, Bronchial [description not available] | 0 | 4.07 | 2 | 1 |
Asthma A form of bronchial disorder with three distinct components: airway hyper-responsiveness (RESPIRATORY HYPERSENSITIVITY), airway INFLAMMATION, and intermittent AIRWAY OBSTRUCTION. It is characterized by spasmodic contraction of airway smooth muscle, WHEEZING, and dyspnea (DYSPNEA, PAROXYSMAL). | 0 | 4.07 | 2 | 1 |
Diffuse Parenchymal Lung Disease [description not available] | 0 | 2.31 | 1 | 0 |
Lung Diseases, Interstitial A diverse group of lung diseases that affect the lung parenchyma. They are characterized by an initial inflammation of PULMONARY ALVEOLI that extends to the interstitium and beyond leading to diffuse PULMONARY FIBROSIS. Interstitial lung diseases are classified by their etiology (known or unknown causes), and radiological-pathological features. | 0 | 2.31 | 1 | 0 |
Chronic Lung Injury [description not available] | 0 | 2.17 | 1 | 0 |
Disease, Pulmonary [description not available] | 0 | 2.17 | 1 | 0 |
Lung Diseases Pathological processes involving any part of the LUNG. | 0 | 2.17 | 1 | 0 |
Disease Exacerbation [description not available] | 0 | 3.5 | 2 | 0 |
Sensitivity and Specificity Binary classification measures to assess test results. Sensitivity or recall rate is the proportion of true positives. Specificity is the probability of correctly determining the absence of a condition. (From Last, Dictionary of Epidemiology, 2d ed) | 0 | 3.76 | 3 | 0 |