Pericardial effusion
Symptom Information:
Symptom ID: | HPO:0001698 | ||||||||||||||||
Synonyms: |
|
||||||||||||||||
Quality: | |||||||||||||||||
Cross references: |
|
||||||||||||||||
Is a (Direct Parents): |
|
||||||||||||||||
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) MedDRA: Cardiac disorders(MedDRA:10007541) Pericardial disorders(MedDRA:10034468) Pericardial disorders NEC(MedDRA:10034469) Pericardial effusion(HPO:0001698) |
||||||||||||||||
Database Frequency: | 20 / 7739 | ||||||||||||||||
Resource: |
All diseases associated with this symptom:
AL amyloidosis | (Orphanet:85443) |
ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS | (OMIM:108050) |
ATTRV122I amyloidosis | (Orphanet:85451) |
Alström syndrome | (Orphanet:64) |
CHOANAL ATRESIA AND LYMPHEDEMA | (OMIM:613611) |
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | (Orphanet:300751) |
Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency | (Orphanet:289527) |
HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITALABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES | (OMIM:614684) |
Hennekam syndrome | (Orphanet:2136) |
Hypertrichotic osteochondrodysplasia, Cantu type | (Orphanet:1517) |
Idiopathic recurrent pericarditis | (Orphanet:251307) |
Lymphangioleiomyomatosis | (Orphanet:538) |
Mucopolysaccharidosis type 2, severe form | (Orphanet:217085) |
Mulibrey nanism | (Orphanet:2576) |
Myhre syndrome | (Orphanet:2588) |
PERICARDIAL EFFUSION, CHRONIC | (OMIM:260900) |
PMM2-CDG | (Orphanet:79318) |
Pediatric systemic lupus erythematosus | (Orphanet:93552) |
Pulmonary venoocclusive disease | (Orphanet:31837) |
Sialidosis type 2 | (Orphanet:87876) |