Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
History of chronic lung disease |
Associated finding |
False |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
1 |
Chronic silicosis |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
History of chronic lung disease |
Associated finding |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
1 |
Chronic lung disease due to surfactant disorder |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Chronic obstructive pulmonary disease |
Is a |
False |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Chronic pulmonary congestion |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Chronic fibrosis of lung |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Chronic nonspecific lung disease |
Is a |
False |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Chronic pulmonary histoplasmosis |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Chronic pulmonary edema |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Chronic induration of lung |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Cystic-bullous disease of the lung |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Chronic atelectasis |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Local recurrence of malignant neoplasm of lung |
Is a |
False |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Chronic pulmonary radiation disease |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Chronic pulmonary aspergillosis |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Chronic bronchiolitis |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Chronic pneumonia |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Chronic respiratory distress with surfactant metabolism deficiency is a rare, genetic, primary interstitial lung disease with a highly variable clinical presentation, ranging from neonatal respiratory distress syndrome to mild to severe interstitial lung disease (typical symptoms include cough, tachypnea, hypoxia, clubbing, crackles, failure to thrive). Lung biopsy reveals diffuse alveolar damage, interstitial thickening with inflammatory infiltrates, fibroblast proliferation, collagen deposition, and multiple foci of fibrosis, alveolar type II cell hyperplasia, abundant foamy alveolar macrophages and granular lipoproteic material in the alveolar lumen. Imaging shows cystic spaces and ground-glass opacities that are typically homogenously diffuse. |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Chronic rejection of lung transplant (disorder) |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Chronic pulmonary coccidioidomycosis |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome is a rare, genetic, hereditary poikiloderma syndrome characterized by early-onset poikiloderma (mainly on the face), hypotrichosis, hypohidrosis, muscle and tendon contractures with varus foot deformity, progressive proximal and distal muscle weakness in all extremities, and progressive pulmonary fibrosis. Mild lymphedema of the extremities, growth retardation, liver impairment, exocrine pancreatic insufficiency and hematologic abnormalities are additional variable features. |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Chronic berylliosis |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Chronic pulmonary insufficiency of prematurity |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Bronchopulmonary dysplasia of newborn (disorder) |
Is a |
False |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Wilson-Mikity syndrome |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Perinatal pulmonary fibroplasia |
Is a |
False |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Perinatal pulmonary fibroplasia |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Pulmonary fibroplasia |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Bronchopulmonary dysplasia of newborn (disorder) |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
A rare genetic respiratory disease characterized by infantile onset of pulmonary alveolar proteinosis with hypogammaglobulinemia. Patients have normal respiratory function at birth, but subsequently develop recurrent, mainly viral, infections and progressive respiratory failure, often leading to death in infancy or early childhood. Additional reported features include leukocytosis and splenomegaly. |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Relapse pulmonary tuberculosis (disorder) |
Is a |
False |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
A rare, genetic interstitial lung disease characterised by accumulation of lipoproteins in the pulmonary alveoli leading to restrictive lung disease and respiratory failure. Patients present with dyspnoea, tachypnoea, cough, failure to thrive, and digital clubbing. Liver disease have been described in some cases including hepatomegaly, steatosis, fibrosis or cirrhosis. |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Pulmonary emphysema |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Disorder characterized by persistent airflow limitation with several features usually associated with asthma and several features usually associated with COPD; identified by the features that it shares with both asthma and COPD. |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Idiopathic chronic eosinophilic pneumonitis |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Chronic endogenous lipoid pneumonitis (disorder) |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Chronic interstitial pneumonitis |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Chronic pneumonitis of infancy (disorder) |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Chronic pulmonary blastomycosis (disorder) |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Acute exacerbation of idiopathic pulmonary fibrosis (disorder) |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
A rare disease, manifesting with idiopathic pulmonary fibrosis, hepatic nodular regenerative hyperplasia leading to portal hypertension and thrombocytopenia due to bone marrow hypoplasia. The condition was associated with 100% mortality. |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Familial idiopathic pulmonary fibrosis (disorder) |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Chronic exogenous lipoid pneumonitis (disorder) |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
A rare interstitial lung disease characterized by early-onset, severe, progressive lung disease manifesting by respiratory distress, neurological symptoms including axial hypotonia, developmental delay, irritability, dystonia, poor visual contact and seizures, and variable multisystemic involvement including malabsorption, progressive growth failure, recurrent infections, chronic hemolytic anemia and liver dysfunction. Kidney dysfunction, cardiac involvement including cardiomegaly and cardiac hypertrophy, decreased vision and strabismus have also been reported. Lung fibrosis may cause death in infancy from respiratory failure. |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|
Lung disease, immunodeficiency, chromosome breakage syndrome (disorder) |
Is a |
True |
Chronic lung disease (disorder) |
Inferred relationship |
Some |
|