FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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Term dilated cardiomyopathy 2D ID (Ontology) DOID:0081160 (Human Disease)
Definition A dilated cardiomyopathy that is characterized by neonatal onset of severe cardiomyopathy, with rapid progression to cardiac decompensation and death unless the patient undergoes heart transplantation and that has_material_basis_in homozygous or compound heterozygous mutation in the RPL3L gene on chromosome 16p13.
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 Genes
 dilated cardiomyopathy 2D       1
 for disease ribbon | dilated cardiomyopathy 2D       1
 model of | dilated cardiomyopathy 2D       1
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autosomal genetic disease
 |__autosomal recessive disease__
intrinsic cardiomyopathy         |
 |__dilated cardiomyopathy_______|
                                 dilated cardiomyopathy 2D  1 rec.
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Is a autosomal recessive disease
dilated cardiomyopathy
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MIM:619371