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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
46,XX Sex Reversal with Dysgenesis of Kidneys, Adrenals, and Lungs  
acute chest syndrome  
adult respiratory distress syndrome  
alpha 1-antitrypsin deficiency  
Alpha-2-Macroglobulin Deficiency 
alveolar echinococcosis  
angiomyolipoma +   
Bacterial Lung Diseases +   
capillariasis 
CHOPS Syndrome  
Congenital Pulmonary Lymphangiectasia 
Cystic Adenomatoid Malformation of Lung, Congenital 
Cystic Disease of Lung  
cystic echinococcosis  
cystic fibrosis +   
dirofilariasis 
Fungal Lung Diseases +   
Hemoptysis 
hepatopulmonary syndrome  
hyperlucent lung 
interstitial lung disease +   
Kashani Strom Utley Syndrome 
lung abscess 
Lung Agenesis +   
Lung Damage, Immunodeficiency and Chromosome Breakage Syndrome  
Lung Injury +   
Lung Neoplasms +   
lymphangioleiomyomatosis  
A lung disease that is characterized by progressive cystic destruction of the lung and lymphatic abnormalities, frequently associated with renal angiomyolipomas. (DO)
maple bark strippers' lung 
middle lobe syndrome  
newborn respiratory distress syndrome +   
obstructive lung disease +   
paracoccidioidomycosis +   
Parasitic Lung Diseases +   
phaeohyphomycosis +  
pneumonia +   
pneumonic plague 
pulmonary alveolar microlithiasis  
pulmonary alveolar proteinosis +   
pulmonary artery disease +   
Pulmonary Atelectasis +   
pulmonary eosinophilia +   
Pulmonary Function 
Pulmonary Hemorrhage +   
pulmonary hemosiderosis 
pulmonary hypertension +   
pulmonary immaturity 
pulmonary plasma cell granuloma  
pulmonary systemic sclerosis 
pulmonary tuberculosis +   
respiratory failure +   
scimitar syndrome +   
sparganosis 
syndromic microphthalmia 9  
toxocariasis +   
uterus perivascular epithelioid cell tumor 

Synonyms
Exact Synonyms: LAM ;   lung lymphangioleiomyomatosis ;   lymphangioleiomyomatoses ;   lymphangiomyomatoses ;   lymphangiomyomatosis ;   pulmonary lymphangioleiomyomatosis
Narrow Synonyms: somatic lymphangioleiomyomatosis
Primary IDs: MESH:D018192
Alternate IDs: MIM:606690
Xrefs: EFO:1000334 ;   GARD:3319 ;   ICDO:9174/1 ;   MONDO:0011705 ;   NCI:C3725 ;   NCI:C38153 ;   ORDO:538
Definition Sources: https://pubmed.ncbi.nlm.nih.gov/31610670/ "DO" "DO"

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