Abnormality of the pericardium

Symptom Information:

Symptom ID: HPO:0001697
Pericardium anomaly [Orphanet:34580]
Pericardial anomaly (disorder) [Orphanet:34580]
Pericardial defect (disorder) [Orphanet:34580]
Congenital anomaly of pericardium (disorder) [Orphanet:34580]
Pericardial anomaly [Orphanet:34580]
Congenital anomaly of pericardium [Orphanet:34580]
Pericardium anomalies/pericarditis/absence/cysts/pericardial effusion [Orphanet:34580]
Pericardium absence [Orphanet:34580]
Totally absent pericardium (disorder) [Orphanet:34580]
Totally absent pericardium [Orphanet:34580]
Pericardial cyst [MedDRA:10051730]
Pericardial cyst [Orphanet:34580]
Pericardial Cyst [Orphanet:34580]
Cross references:
Orphanet:34580 "Pericardium anomalies/pericarditis/absence/cysts/pericardial effusion" [Orphanet:34580]
UMLS:C0345138 "Pericardial anomaly" [Orphanet:34580]
UMLS:C0685699 "Congenital anomaly of pericardium" [Orphanet:34580]
UMLS:C0345140 "Totally absent pericardium" [Orphanet:34580]
UMLS:C0031038 "Pericardial Cyst" [Orphanet:34580]
Is a (Direct Parents):
HPO         obsolete Malformation of the heart and great vessels
Orphanet Structural anomalies of the cardio-circulatory system
Is a (Whole tree): HPO:
    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)
Database Frequency: 52 / 7739

All diseases associated with this symptom:

Adult Still's disease (Orphanet:829)
Beh├žet 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)