Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
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Infection (D007239)
Parent Node:
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Respiratory Tract Diseases (D012140)
..Starting node
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Respiratory Tract Infections (D012141)

       Child 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)



 Sister Nodes: 
..expandBronchial Diseases (D001982) Child54
..expandCiliary Motility Disorders (D002925) Child21
..expandCutis Laxa With Severe Pulmonary, Gastrointestinal, And Urinary Abnormalities (C567716)
..expandGranuloma, Respiratory Tract (D015769) Child1
..expandLaryngeal Diseases (D007818) Child37
..expandLung Diseases (D008171) Child190
..expandNose Diseases (D009668) Child42
..expandPleural Diseases (D010995) Child19
..expandRespiration Disorders (D012120) Child65
..expandRespiratory Hypersensitivity (D012130) Child30
..expandRespiratory System Abnormalities (D015619) Child27
..expandRespiratory Tract Fistula (D016156) Child6
..expandRespiratory Tract Infections (D012141) Child75
..expandRespiratory Tract Neoplasms (D012142) Child30
..expandSiegler Brewer Carey syndrome (C537335)
..expandThoracic Diseases (D013896) Child7
..expandTracheal Diseases (D014133) Child19
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:9694
Name:Respiratory Tract Infections
Definition:Invasion of the host RESPIRATORY SYSTEM by microorganisms, usually leading to pathological processes or diseases.
Alternative IDs:
ParentIDs:MESH:D007239|MESH:D012140
TreeNumbers:C01.539.739 |C08.730
Synonyms:Infection, Respiratory Tract |Infections, Respiratory |Infections, Respiratory Tract |Infections, Upper Respiratory |Infections, Upper Respiratory Tract |Respiratory Infections |Respiratory Infection, Upper |Respiratory Tract Infection |Upper Respiratory Infecti
Slim Mappings:Bacterial infection or mycosis|Respiratory tract disease
Reference: MedGen: D012141
MeSH: D012141
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants