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familial isolated arrhythmogenic ventricular dysplasia, right dominant form - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

familial isolated arrhythmogenic ventricular dysplasia, right dominant form

MONDO:0017403

Also known as:familial isolated arrhythmogenic ventricular cardiomyopathy, classic formfamilial isolated arrhythmogenic ventricular cardiomyopathy, right dominant formfamilial isolated arrhythmogenic ventricular dysplasia, classic form

Overview

ResearchLimited published research (1 article)

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 familial isolated arrhythmogenic ventricular dysplasia, right dominant form.

1 publication has been identified in PubMed for familial isolated arrhythmogenic ventricular dysplasia, right dominant form. Research spans Basic Science / Preclinical (100%).

Recent Publications

Vanaja IP (2025). [PMID: 39141822](https://pubmed.ncbi.nlm.nih.gov/39141822/). *J Physiol*. [Basic Science / Preclinical]

Data assembled from 3 of 12 sources · Last updated Sep 18, 2026, 8:14 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:293910

GARD

Genetic and Rare Diseases Info Center

GARD:17347

Questions for Your Care Team

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familial isolated arrhythmogenic ventricular dysplasia, right dominant form

Overview

Research Landscape

Recent Publications

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team