Pleural effusion

Symptom Information:

Symptom ID: HPO:0002202
Synonyms:
Pleural effusion (disorder) [Orphanet:32520]
Pleural effusion disorder [Orphanet:32520]
Pleural effusion [OMIM:Pleural effusion]
Abnormal pleura/hydrothorax/pleuresia/pleural effusion/chylothorax [Orphanet:32520]
Pleural effusion [Orphanet:32520]
Pleural effusion [MedDRA:10035598]
Effusion pleural [MedDRA:10035598]
Intrapleural fluid retention of [MedDRA:10035598]
Other specified forms of pleural effusion, except tuberculous [MedDRA:10035598]
Unspecified pleural effusion [MedDRA:10035598]
Pleural fluid exudate [MedDRA:10035598]
Pulmonary effusion [MedDRA:10035598]
Pleural effusion recurrent [MedDRA:10035598]
Trapped lung [MedDRA:10035598]
Pleural effusions [OMIM:Pleural effusions]
Hydrothorax [MedDRA:10048612]
Hydrothorax (disorder) [Orphanet:32520]
Hydrothorax [Orphanet:32520]
Hydrothorax [OMIM:Hydrothorax]
Quality:
Cross references:
Orphanet:32520 "Abnormal pleura/hydrothorax/pleuresia/pleural effusion/chylothorax" [Orphanet:32520]
OMIM: "Pleural effusion" [OMIM:Pleural effusion]
OMIM: "Pleural effusions" [OMIM:Pleural effusions]
OMIM: "Hydrothorax" [OMIM:Hydrothorax]
UMLS:C0032227 "Pleural effusion disorder" [Orphanet:32520]
UMLS:C0020312 "Hydrothorax" [Orphanet:32520]
Is a (Direct Parents):
Orphanet Abnormality of the diaphragm
MedDRA Pneumothorax and pleural effusions NEC
Orphanet Pleuritis
HPO         Abnormality of the pleura
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)
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)