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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Respiratory Tract Diseases (D012140)
..Starting node
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Lung Diseases (D008171)

       Child Nodes:
........expand46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS (OMIM:611812)
........expandAcute Chest Syndrome (D056586)
........expandalpha 1-Antitrypsin Deficiency (D019896) Child1
........expandalpha-2-Macroglobulin Deficiency (C566304)
........expandAnophthalmia with pulmonary hypoplasia (C537768)
........expandCystic Adenomatoid Malformation of Lung, Congenital (D015615)
........expandCystic Disease Of Lung (C563237)
........expandCystic Fibrosis (D003550) Child4
........expandHemoptysis (D006469)
........expandHepatopulmonary Syndrome (D020065)
........expandHypertension, Pulmonary (D006976) Child12
........expandIdiopathic pulmonary hemosiderosis (C536281)
........expandKashani Strom Utley syndrome (C537010)
........expandLung Abscess (D008169)
........expandLung agenesis (C537725)
........expandLung Diseases, Fungal (D008172) Child5
........expandLung Diseases, Interstitial (D017563) Child39
........expandLung Diseases, Obstructive (D008173) Child34
........expandLung Diseases, Parasitic (D008174) Child1
........expandLung Injury (D055370) Child20
........expandLung Neoplasms (D008175) Child17
........expandLung, Hyperlucent (D019568)
........expandLymphangiectasia, pulmonary, congenital (C537727)
........expandPlasma Cell Granuloma, Pulmonary (D016726)
........expandPneumonia (D011014) Child16
........expandPulmonary Alveolar Microlithiasis (C562405)
........expandPulmonary Alveolar Proteinosis (D011649) Child7
........expandPulmonary Atelectasis (D001261) Child1
........expandPulmonary Edema (D011654) Child1
........expandPulmonary Embolism (D011655) Child3
........expandPulmonary Eosinophilia (D011657) Child1
........expandPulmonary Fibrosis (D011658) Child2
........expandPULMONARY FUNCTION (OMIM:608852)
........expandPulmonary Hypoplasia, Primary (C562992)
........expandPulmonary Veno-Occlusive Disease (D011668)
........expandRapidly progressive glomerulonephritis with pulmonary hemorrhage (C538458)
........expandRespiratory Distress Syndrome, Adult (D012128)
........expandRespiratory Distress Syndrome, Newborn (D012127) Child9
........expandScimitar Syndrome (D012587) Child1
........expandSolitary Pulmonary Nodule (D003074)
........expandTetra-amelia with pulmonary hypoplasia (C536499)
........expandTuberculosis, Pulmonary (D014397) Child1



 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:6561
Name:Lung Diseases
Definition:Pathological processes involving any part of the LUNG.
Alternative IDs:
ParentIDs:MESH:D012140
TreeNumbers:C08.381
Synonyms:Disease, Lung |Disease, Pulmonary |Diseases, Lung |Diseases, Pulmonary |Lung Disease |Pulmonary Disease |Pulmonary Diseases
Slim Mappings:Respiratory tract disease
Reference: MedGen: D008171
MeSH: D008171
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants