Serous pericardial effusion

Symptom Information:

Symptom ID: HPO:0011853
Synonyms:
Pericardial effusion [Orphanet:34580]
Pericardial effusion (disorder) [Orphanet:34580]
Pericardium anomalies/pericarditis/absence/cysts/pericardial effusion [Orphanet:34580]
Pericardial effusion [MedDRA:10034474]
Effusion pericardial [MedDRA:10034474]
Pericardial fluid exudate [MedDRA:10034474]
Pericardial effusion (in some patients) [OMIM:Pericardial effusion (in some patients)]
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]
Quality:
Cross references:
HPO:0001698 "Pericardial effusion" [Orphanet:34580]
Orphanet:34580 "Pericardium anomalies/pericarditis/absence/cysts/pericardial effusion" [Orphanet:34580]
OMIM: "Pericardial effusion (in some patients)" [OMIM:Pericardial effusion (in some patients)]
UMLS:C0031039 "Pericardial effusion" [Orphanet:34580]
UMLS:C0345140 "Totally absent pericardium" [Orphanet:34580]
UMLS:C0031038 "Pericardial Cyst" [Orphanet:34580]
Is a (Direct Parents):
HPO         Pericardial effusion
MedDRA Pericardial disorders NEC
Orphanet Structural anomalies of the cardio-circulatory system
Orphanet Abnormality of the pericardium
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)
                   Pericardial effusion(HPO:0001698)
                      Serous pericardial effusion(HPO:0011853)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Pericardial disorders(MedDRA:10034468)
       Pericardial disorders NEC(MedDRA:10034469)
          Serous pericardial effusion(HPO:0011853)
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Familial dilated cardiomyopathy with conduction defect due to LMNA mutation (Orphanet:300751)
HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITALABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES (OMIM:614684)
Lymphangioleiomyomatosis (Orphanet:538)