Pulmonary embolism

Symptom Information:

Symptom ID: HPO:0002204
Synonyms:
Pulmonary embolism (disorder) [Orphanet:35330]
Pulmonary thrombosis (disorder) [Orphanet:35330]
Pulmonary thromboembolism (disorder) [Orphanet:35330]
Pulmonary Thromboembolisms [Orphanet:35330]
Pulmonary thrombosis [Orphanet:35330]
Pulmonary Embolism [Orphanet:35330]
Pulmonary embolism [OMIM:Pulmonary embolism]
Pulmonary thromboembolism [Orphanet:35330]
Pulmonary embolism [Orphanet:35330]
Pulmonary embolism [MedDRA:10037377]
Acute massive pulmonary embolism [MedDRA:10037377]
Acute P.E. [MedDRA:10037377]
Chronic P.E. [MedDRA:10037377]
Chronic pulmonary embolism [MedDRA:10037377]
Embolism pulmonary [MedDRA:10037377]
Embolus pulmonary [MedDRA:10037377]
Multiple PE's [MedDRA:10037377]
PE [MedDRA:10037377]
Pulmonary embolus [MedDRA:10037377]
Pulmonary thromboembolism [MedDRA:10037377]
Saddle PE [MedDRA:10037377]
Embolism lung [MedDRA:10037377]
Recurrent pulmonary embolism [MedDRA:10037377]
Emboli, pulmonary (in some patients) [OMIM:Emboli, pulmonary (in some patients)]
Pulmonary emboli [OMIM:Pulmonary emboli]
Pulmonary thrombosis [MedDRA:10037437]
Quality:
Cross references:
Orphanet:35330 "Pulmonary thromboembolism" [Orphanet:35330]
OMIM: "Pulmonary embolism" [OMIM:Pulmonary embolism]
OMIM: "Emboli, pulmonary (in some patients)" [OMIM:Emboli, pulmonary (in some patients)]
OMIM: "Pulmonary emboli" [OMIM:Pulmonary emboli]
UMLS:C0524702 "Pulmonary Thromboembolisms" [Orphanet:35330]
UMLS:C0151946 "Pulmonary thrombosis" [Orphanet:35330]
UMLS:C0034065 "Pulmonary Embolism" [Orphanet:35330]
Is a (Direct Parents):
Orphanet Abnormality of cardiovascular system physiology
HPO         Abnormality of lung morphology
MedDRA Pulmonary thrombotic and embolic conditions
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the respiratory system(HPO:0002086)
          Abnormal respiratory system morphology(HPO:0012252)
             Abnormality of lung morphology(HPO:0002088)
                Pulmonary embolism(HPO:0002204)
MedDRA:
Respiratory, thoracic and mediastinal disorders(MedDRA:10038738)
    Pulmonary vascular disorders(MedDRA:10037454)
       Pulmonary thrombotic and embolic conditions(MedDRA:10037439)
          Pulmonary embolism(HPO:0002204)
Database Frequency: 26 / 7739
Resource:

All diseases associated with this symptom:

48,XXXY syndrome (Orphanet:96263)
49,XXXXY syndrome (Orphanet:96264)
Angio-osteohypertrophic syndrome (Orphanet:2346)
Behçet disease (Orphanet:117)
Cardiomyopathy, dilated, 1S (OMIM:613426)
Cardiomyopathy-cataract-hip spine disease (Orphanet:1345)
Classical homocystinuria (Orphanet:394)
FACTOR V EXCESS WITH SPONTANEOUS THROMBOSIS (OMIM:134400)
Familial multiple nevi flammei (Orphanet:624)
Hereditary hemorrhagic telangiectasia (Orphanet:774)
Hereditary thrombophilia due to congenital antithrombin deficiency (Orphanet:82)
Hereditary thrombophilia due to congenital protein C deficiency (Orphanet:745)
Hereditary thrombophilia due to congenital protein S deficiency (Orphanet:743)
Hughes-Stovin syndrome (Orphanet:228116)
Klippel-Trénaunay syndrome (Orphanet:90308)
Left ventricular noncompaction (Orphanet:54260)
MELAS (Orphanet:550)
Papillary fibroelastoma of the heart (Orphanet:208600)
Protein S acquired deficiency (Orphanet:26349)
Proteus syndrome (Orphanet:744)
Recessive mitochondrial ataxia syndrome (Orphanet:94125)
Spastic paraplegia type 2 (Orphanet:99015)
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL DOMINANT (OMIM:176860)
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE (OMIM:612304)
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE (OMIM:614514)
THROMBOPHILIA DUE TO THROMBIN DEFECT (OMIM:188050)