Abnormality of the pericardium
Symptom Information:
Symptom ID: | HPO:0001697 | |||||||||||||
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 cardiovascular system(HPO:0001626) Abnormal heart morphology(HPO:0001627) obsolete Malformation of the heart and great vessels(HPO:0002564) Abnormality of the pericardium(HPO:0001697) MedDRA: |
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Database Frequency: | 52 / 7739 | |||||||||||||
Resource: |
All diseases associated with this symptom:
Adult Still's disease | (Orphanet:829) |
Behçet disease | (Orphanet:117) |
Blau syndrome | (Orphanet:90340) |
CEDNIK syndrome | (Orphanet:66631) |
CREST syndrome | (Orphanet:90290) |
Cantrell pentalogy | (Orphanet:1335) |
Cogan syndrome | (Orphanet:1467) |
Congenital disorder of glycosylation | (Orphanet:137) |
Congenital hypothyroidism | (Orphanet:442) |
Congenital pericardium anomaly | (Orphanet:2846) |
Congenital pulmonary lymphangiectasia | (Orphanet:2414) |
Dermatomyositis | (Orphanet:221) |
Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
Erdheim-Chester disease | (Orphanet:35687) |
Familial Mediterranean fever | (Orphanet:342) |
Felty syndrome | (Orphanet:47612) |
Gaucher disease | (Orphanet:355) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 3 | (Orphanet:77261) |
Giant cell arteritis | (Orphanet:397) |
Granulomatosis with polyangiitis | (Orphanet:900) |
Hb Bart's hydrops fetalis | (Orphanet:163596) |
Hemorrhagic fever - renal syndrome | (Orphanet:340) |
Hennekam syndrome | (Orphanet:2136) |
Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
Intestinal lymphangiectasia | (Orphanet:36204) |
Juvenile dermatomyositis | (Orphanet:93672) |
Juvenile idiopathic arthritis | (Orphanet:92) |
Kawasaki disease | (Orphanet:2331) |
Legionellosis | (Orphanet:549) |
Lymphangioleiomyomatosis | (Orphanet:538) |
Malignant atrophic papulosis | (Orphanet:679) |
Microscopic polyangiitis | (Orphanet:727) |
Mixed connective tissue disease | (Orphanet:809) |
Mulibrey nanism | (Orphanet:2576) |
Multiple osteochondromas | (Orphanet:321) |
Pericardial and diaphragmatic defect | (Orphanet:2847) |
Polyarteritis nodosa | (Orphanet:767) |
Polymyositis | (Orphanet:732) |
Primary effusion lymphoma | (Orphanet:48686) |
Primary intestinal lymphangiectasia | (Orphanet:90362) |
Reactive arthritis | (Orphanet:29207) |
Relapsing polychondritis | (Orphanet:728) |
Rheumatic fever | (Orphanet:3099) |
Scleroderma | (Orphanet:801) |
Sternal malformation - vascular dysplasia | (Orphanet:3195) |
Systemic capillary leak syndrome | (Orphanet:188) |
Systemic-onset juvenile idiopathic arthritis | (Orphanet:85414) |
TRAPS syndrome | (Orphanet:32960) |
Thymic tumor | (Orphanet:100100) |
Thymoma | (Orphanet:99867) |
Whipple disease | (Orphanet:3452) |