Hearing Loss Disease Portal


 
Switch to table view
Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expand
Lung Diseases (D008171)
Parent Node:
expand
Respiratory Tract Infections (D012141)
..Starting node
..expand
Pneumonia (D011014)

       Child Nodes:
........expandBronchopneumonia (D001996)
........expandCholesterol pneumonia (C535937)
........expandPleuropneumonia (D011001)
........expandPneumonia, Aspiration (D011015) Child1
........expandPneumonia, Bacterial (D018410) Child7
........expandPneumonia, Pneumocystis (D011020)
........expandPneumonia, Ventilator-Associated (D053717)
........expandPneumonia, Viral (D011024)



 Sister Nodes: 
..expandBovine Respiratory Disease Complex (D048090) Child3
..expandBronchitis (D001991) Child7
..expandCommon Cold (D003139)
..expandEmpyema, Pleural (D016724) Child1
..expandInfluenza, Human (D007251)
..expandInhalation anthrax (C571912)
..expandLaryngitis (D007827) Child1
..expandLegionellosis (D007876) Child1
..expandLung Abscess (D008169)
..expandLung Diseases, Fungal (D008172) Child5
..expandLung Diseases, Parasitic (D008174) Child1
..expandPharyngitis (D010612) Child4
..expandPleurisy (D010998) Child1
..expandPneumonia (D011014) Child16
..expandRecurrent respiratory papillomatosis (C535297)
..expandRetinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness (C567595)
..expandRhinitis (D012220) Child6
..expandRhinoscleroma (D012226)
..expandSevere Acute Respiratory Syndrome (D045169)
..expandSinusitis (D012852) Child5
..expandSupraglottitis (D059525) Child1
..expandTracheitis (D014136)
..expandTuberculosis, Laryngeal (D014387)
..expandTuberculosis, Pleural (D014396) Child1
..expandTuberculosis, Pulmonary (D014397) Child1
..expandWhooping Cough (D014917)
..expandYoung Syndrome (C536718)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:9022
Name:Pneumonia
Definition:Inflammation of any part, segment or lobe, of the lung parenchyma.
Alternative IDs:
ParentIDs:MESH:D008171|MESH:D012141
TreeNumbers:C08.381.677 |C08.730.610
Synonyms:Experimental Lung Inflammation |Experimental Lung Inflammations |Inflammation, Experimental Lung |Inflammation, Lung |Inflammation, Pulmonary |Inflammations, Lung |Inflammations, Pulmonary |Lobar Pneumonia |Lung Inflammation |Lung Inflammation, Experimental |Lung
Slim Mappings:Respiratory tract disease
Reference: MedGen: D011014
MeSH: D011014
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants