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congenital pericardium anomaly - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

congenital pericardium anomaly

MONDO:0017300

Overview

Congenital pericardium anomaly comprises a group of rare congenital cardiac malformations characterized by the complete (Congenital complete agenesis of pericardium) or partial absence of the pericardium (Congenital partial agenesis of pericardium), or by the presence of pericardial cysts (Pleuropericardial cyst).

Diagnosis

Biomarker and diagnostic research for congenital pericardium anomaly has been reported in the published literature.

Prognosis

Estimated prevalence: Unknown (Unknown prevalence).

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for congenital pericardium anomaly.

55 publications have been identified in PubMed for congenital pericardium anomaly. Research spans Case Report / Case Series (83%), Review / Meta-Analysis (7%), and Basic Science / Preclinical (4%).

Research Type	Count	% of Total
Patient case studies	45	83%

Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 5:49 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:2846

GARD

Genetic and Rare Diseases Info Center

GARD:18779

Questions for Your Care Team

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congenital pericardium anomaly

Overview

Diagnosis

Prognosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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