Pulmonary embolism
Symptom Information:
Symptom ID: | HPO:0002204 | ||||||||||||||||||||||||||
Synonyms: |
|
||||||||||||||||||||||||||
Quality: | |||||||||||||||||||||||||||
Cross references: |
|
||||||||||||||||||||||||||
Is a (Direct Parents): |
|
||||||||||||||||||||||||||
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) |