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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
sarcoidosis +     
autoimmune interstitial lung, joint, and kidney disease  
bronchiolitis obliterans +   
cardiac sarcoidosis 
desquamative interstitial pneumonia  
Early-Onset Sarcoidosis +   
extrinsic allergic alveolitis +   
Goodpasture syndrome +   
granulomatosis with polyangiitis +   
hypercalcemic sarcoidosis 
idiopathic interstitial pneumonia +   
INTERSTITIAL LUNG AND LIVER DISEASE  
interstitial lung disease 1  
Junctional Epidermolysis Bullosa 7, with Interstitial Lung Disease and Nephrotic Syndrome  
Langerhans-cell histiocytosis +   
neurosarcoidosis +  
ocular sarcoidosis 
pneumoconiosis +   
pulmonary fibrosis +   
pulmonary sarcoidosis +   
A sarcoidosis that is characterized by noncaseating granulomatous infiltration of the lungs and supporting lymph nodes, bilateral hilar adenopathy, and pulmonary issues, has_symptom shortness of breath, fatigue, wheezing, and chronic cough, and develops_from a type IV hypersensitivity reaction. (DO)
Pulmonary Surfactant Metabolism Dysfunction 1  
Pulmonary Surfactant Metabolism Dysfunction 2  
Pulmonary Surfactant Metabolism Dysfunction 3  
Pulmonary Surfactant Metabolism Dysfunction 5  
Radiation Pneumonitis  
Rajab Interstitial Lung Disease with Brain Calcifications +   
rheumatoid arthritis interstitial lung disease 
skin sarcoidosis 
Surfactant Dysfunction  
uveoparotid fever  

Synonyms
Exact Synonyms: lung sarcoidosis ;   pulmonary sarcoidoses
Primary IDs: MESH:D017565
Xrefs: ICD10CM:D86.0 ;   NCI:C34997
Definition Sources: https://www.atsjournals.org/doi/full/10.1164/rccm.201006-0865CI "DO" "DO"

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