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Inherited isolated arrhythmogenic cardiomyopathy, dominant-right variant
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ORPHA:293910
Classification level: Subtype of disorder
Synonym(s):
- Arrhythmogenic cardiomyopathy dominant-right variant
- Arrhythmogenic cardiomyopathy with right ventricular involvement
- Familial isolated arrhytmogenic ventricular dysplasia, right dominant form
Source: PubMed ID 32561223
Prevalence: -
Inheritance: Autosomal dominant
Age of onset:
Summary
This disease is described under Inherited isolated arrhythmogenic cardiomyopathy
Detailed information
: produced/endorsed by ERN(s)
: produced/endorsed by FSMR(s)
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Review article
Clinical genetics review
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Guidance for genetic testing
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Further information on this disease
Patient-centred resources for this disease
Research activities on this disease
- Research project(s) (42)
- Clinical trial(s) (3)
- Biobank(s) (11)
- Registry(ies) (26)
- Network of experts (4)
Newborn screening
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