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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Embolism (D004617)
Parent Node:
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Lung Diseases (D008171)
..Starting node
..expand
Pulmonary Embolism (D011655)

       Child Nodes:
........expandPULMONARY HYPERTENSION, CHRONIC THROMBOEMBOLIC, WITHOUT DEEP VEIN THROMBOSIS, SUSCEPTIBILITY TO (OMIM:612862)
........expandPulmonary Infarction (D054060)
........expandSchimke immunoosseous dysplasia (C536629)



 Sister 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
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:9487
Name:Pulmonary Embolism
Definition:Blocking of the PULMONARY ARTERY or one of its branches by an EMBOLUS.
Alternative IDs:
ParentIDs:MESH:D004617|MESH:D008171
TreeNumbers:C08.381.746 |C14.907.355.350.700
Synonyms:Embolism, Pulmonary |Embolisms, Pulmonary |Pulmonary Embolisms |Pulmonary Thromboembolism |Pulmonary Thromboembolisms |Thromboembolism, Pulmonary |Thromboembolisms, Pulmonary
Slim Mappings:Cardiovascular disease|Respiratory tract disease
Reference: MedGen: D011655
MeSH: D011655
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants