Pleural effusion
Symptom Information:
Symptom ID: | HPO:0002202 | |||||||||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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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) Abnormality of the pleura(HPO:0002103) Pleural effusion(HPO:0002202) MedDRA: Respiratory, thoracic and mediastinal disorders(MedDRA:10038738) Pleural disorders(MedDRA:10035597) Pneumothorax and pleural effusions NEC(MedDRA:10035761) Pleural effusion(HPO:0002202) |
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Database Frequency: | 22 / 7739 | |||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS | (OMIM:108050) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cardiomyopathy, familial restrictive 2 | (OMIM:609578) |
Congenital pulmonary lymphangiectasia | (Orphanet:2414) |
Costello syndrome | (Orphanet:3071) |
Cryptogenic organizing pneumonia | (Orphanet:1302) |
Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
Fetal Gaucher disease | (Orphanet:85212) |
Greenberg dysplasia | (Orphanet:1426) |
Hemochromatosis, type 1 | (OMIM:235200) |
Hennekam syndrome | (Orphanet:2136) |
Hereditary chronic pancreatitis | (Orphanet:676) |
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation | (Orphanet:324525) |
Lymphangioleiomyomatosis | (Orphanet:538) |
Malignant atrophic papulosis | (Orphanet:679) |
Mulibrey nanism | (Orphanet:2576) |
Noonan syndrome | (Orphanet:648) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
Pediatric systemic lupus erythematosus | (Orphanet:93552) |
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency | (Orphanet:88618) |
Pulmonary capillary hemangiomatosis | (Orphanet:199241) |
Pulmonary venoocclusive disease | (Orphanet:31837) |