Details of Disease | DrugMAP

General Information of Disease (ID: DIS9VTGJ)

Disease Name	Arrhythmogenic right ventricular dysplasia, familial, 14
Synonyms	ARVD14; Arrhythmogenic Right Ventricular Cardiomyopathy 14; arrhythmogenic right ventricular dysplasia, familial, 14; ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 14
Disease Hierarchy	DISBIOAZ: Familial isolated arrhythmogenic right ventricular dysplasia DIS9VTGJ: Arrhythmogenic right ventricular dysplasia, familial, 14
Disease Identifiers	MONDO ID MONDO_0030062 UMLS CUI C5394505 OMIM ID 618920 MedGen ID 1712001

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
CDH2	TT1WS0T	Strong	Autosomal dominant	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
CDH2	OTH0Y56P	Strong	Autosomal dominant	[1]
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References

1	Identification of Cadherin 2 (CDH2) Mutations in Arrhythmogenic Right Ventricular Cardiomyopathy. Circ Cardiovasc Genet. 2017 Apr;10(2):e001605. doi: 10.1161/CIRCGENETICS.116.001605.