Abnormality of the pleura

Symptom Information:

Symptom ID: HPO:0002103
Synonyms:
Pleural cavity anomaly [Orphanet:32520]
Anomaly of pleura (disorder) [Orphanet:32520]
Anomaly of pleura [Orphanet:32520]
Abnormal pleura/hydrothorax/pleuresia/pleural effusion/chylothorax [Orphanet:32520]
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: "Hydrothorax" [OMIM:Hydrothorax]
UMLS:C0431544 "Anomaly of pleura" [Orphanet:32520]
UMLS:C0020312 "Hydrothorax" [Orphanet:32520]
Is a (Direct Parents):
Orphanet Abnormality of the diaphragm
Orphanet Pleuritis
HPO         Abnormality of lung morphology
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)
MedDRA:
Database Frequency: 58 / 7739
Resource:

All diseases associated with this symptom:

Adult Still's disease (Orphanet:829)
Arthrogryposis multiplex congenita (Orphanet:1037)
Behçet disease (Orphanet:117)
Castleman disease (Orphanet:160)
Cogan syndrome (Orphanet:1467)
Congenital pulmonary airway malformation (Orphanet:2444)
Congenital pulmonary lymphangiectasia (Orphanet:2414)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Erdheim-Chester disease (Orphanet:35687)
Familial Mediterranean fever (Orphanet:342)
Familial dysautonomia (Orphanet:1764)
Familial spontaneous pneumothorax (Orphanet:2903)
Felty syndrome (Orphanet:47612)
Follicular lymphoma (Orphanet:545)
Giant cell arteritis (Orphanet:397)
Gorlin syndrome (Orphanet:377)
Granulomatosis with polyangiitis (Orphanet:900)
Hemorrhagic fever - renal syndrome (Orphanet:340)
Hennekam syndrome (Orphanet:2136)
Hydatidosis (Orphanet:400)
Hypocomplementemic urticarial vasculitis (Orphanet:36412)
Hypotrichosis - lymphedema - telangiectasia (Orphanet:69735)
Idiopathic acute eosinophilic pneumonia (Orphanet:724)
Intestinal lymphangiectasia (Orphanet:36204)
Juvenile idiopathic arthritis (Orphanet:92)
Lassa fever (Orphanet:99824)
Legionellosis (Orphanet:549)
Lyell syndrome (Orphanet:537)
Lymphangioleiomyomatosis (Orphanet:538)
Lymphoid interstitial pneumonia (Orphanet:79128)
Malignant atrophic papulosis (Orphanet:679)
Microcephaly - lymphedema - chorioretinopathy (Orphanet:2526)
Mixed connective tissue disease (Orphanet:809)
Morse-Rawnsley-Sargent syndrome (Orphanet:2570)
Mucopolysaccharidosis type 7 (Orphanet:584)
Myalgia-eosinophilia syndrome associated with tryptophan (Orphanet:2582)
Non-specific interstitial pneumonia (Orphanet:91364)
Primary effusion lymphoma (Orphanet:48686)
Primary intestinal lymphangiectasia (Orphanet:90362)
Pulmonary blastoma (Orphanet:64741)
Radio-renal syndrome (Orphanet:3015)
Reactive arthritis (Orphanet:29207)
Respiratory bronchiolitis - interstitial lung disease (Orphanet:79127)
Rheumatic fever (Orphanet:3099)
Secondary intestinal lymphangiectasia (Orphanet:90363)
Stevens-Johnson syndrome (Orphanet:36426)
Systemic capillary leak syndrome (Orphanet:188)
Systemic-onset juvenile idiopathic arthritis (Orphanet:85414)
Sézary syndrome (Orphanet:3162)
TRAPS syndrome (Orphanet:32960)
Thymic carcinoma (Orphanet:99868)
Thymoma (Orphanet:99867)
Tuberous sclerosis (Orphanet:805)
Waldenström macroglobulinemia (Orphanet:33226)
Whipple disease (Orphanet:3452)
X-linked immunoneurologic disorder (Orphanet:2571)
Yellow nail syndrome (Orphanet:662)