FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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Term dilated cardiomyopathy 2E ID (Ontology) DOID:0081161 (Human Disease)
Definition A dilated cardiomyopathy that is characterized by neonatal or early childhood onset of dilated cardiomyopathy, with rapid progression to cardiac failure and death unless patients undergo cardiac transplantation and that has_material_basis_in homozygous or compound heterozygous mutation in the JPH2 gene on chromosome 20q13.
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 Genes
 dilated cardiomyopathy 2E       1
 for disease ribbon | dilated cardiomyopathy 2E       1
 model of | dilated cardiomyopathy 2E       1
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autosomal genetic disease
 |__autosomal recessive disease__
intrinsic cardiomyopathy         |
 |__dilated cardiomyopathy_______|
                                 dilated cardiomyopathy 2E  1 rec.
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Is a autosomal recessive disease
dilated cardiomyopathy
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MIM:619492