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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
histiocytosis +     
interstitial lung disease +     
autoimmune interstitial lung, joint, and kidney disease  
bronchiolitis obliterans +   
desquamative interstitial pneumonia  
extrinsic allergic alveolitis +   
Familial Lipochrome Histiocytosis 
Goodpasture syndrome +   
granulomatosis with polyangiitis +   
histiocytosis-lymphadenopathy plus syndrome  
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 +   
A histiocytosis that is characterized by clonal proliferation of Langerhans cells. (DO)
malignant histiocytic disease +   
non-Langerhans-cell histiocytosis +   
pneumoconiosis +   
Progressive Mucinous Histiocytosis 
pulmonary fibrosis +   
pulmonary sarcoidosis +   
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 
Surfactant Dysfunction  

Synonyms
Exact Synonyms: Generalized Histiocytosis ;   Hand Schueller Christian Disease ;   Hand Schueller Christian Syndrome ;   Hand Schüller Christian Disease ;   Hand Schüller Christian Syndrome ;   Hashimoto-Pritzger Disease ;   Histiocytosis X ;   Langerhan's cell histiocytosis ;   Langerhans Cell Granulomatosis ;   Langerhans cell granulomatoses ;   Langerhans cell histiocytoses ;   Letterer Siwe Disease ;   Letterer-Siwe disease involving intra-abdominal lymph nodes ;   Letterer-Siwe disease involving intrapelvic lymph nodes ;   Letterer-Siwe disease involving intrathoracic lymph nodes ;   Letterer-Siwe disease involving lymph nodes of axilla and upper limb ;   Letterer-Siwe disease involving lymph nodes of head, face, and neck ;   Letterer-Siwe disease involving lymph nodes of inguinal region and lower limb ;   Letterer-Siwe disease involving lymph nodes of multiple sites ;   Letterer-Siwe disease involving spleen ;   Letterer-Siwe disease of intra-abdominal lymph nodes ;   Letterer-Siwe disease of intrapelvic lymph nodes ;   Letterer-Siwe disease of intrathoracic lymph nodes ;   Letterer-Siwe disease of lymph nodes of axilla and upper limb ;   Letterer-Siwe disease of lymph nodes of axilla and/or upper limb ;   Letterer-Siwe disease of lymph nodes of head, face and neck ;   Non Lipid Reticuloendotheliosis ;   Non-Lipid Reticuloendothelioses ;   Pulmonary Histiocytosis X ;   Pulmonary Langerhans Cell Granulomatosis ;   Schueller Christian Disease ;   Systemic Aleukemic Reticuloendothelioses ;   generalized histiocytoses ;   systemic aleukemic reticuloendotheliosis ;   type 2 histiocytoses ;   type 2 histiocytosis
Narrow Synonyms: Letterer-Siwe disease of lymph nodes of head, face and/or neck ;   Letterer-Siwe disease of lymph nodes of inguinal region amd/or lower limb ;   Letterer-Siwe disease of lymph nodes of inguinal region and lower limb ;   Letterer-Siwe disease of lymph nodes of inguinal region and/or lower limb ;   Letterer-Siwe disease of lymph nodes of multiple sites ;   Letterer-Siwe disease of spleen
Primary IDs: MESH:D006646
Alternate IDs: OMIM:604856
Xrefs: EFO:1000318 ;   ICD10CM:C96.0 ;   ICD10CM:C96.6 ;   ICD9CM:202.5 ;   NCI:C158785 ;   NCI:C3107 ;   NCI:C3160 ;   NCI:C6920
Definition Sources: http://en.wikipedia.org/wiki/Langerhans_cell_histiocytosis "DO" "DO"

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