Abnormality of the pleura
Symptom Information:
Symptom ID: | HPO:0002103 | ||||||||
Synonyms: |
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Quality: | |||||||||
Cross references: |
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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) MedDRA: |
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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) |