FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
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Term dilated cardiomyopathy 2G ID (Ontology) DOID:0081163 (Human Disease)
Definition A dilated cardiomyopathy that is characterized by early-onset severe dilated cardiomyopathy that progresses rapidly to heart failure in the neonatal period without evidence of intervening hypertrophy and that has_material_basis_in homozygous or compound heterozygous mutation in the LMOD2 gene on chromosome 7q31.
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 Genes
 dilated cardiomyopathy 2G       1
 for disease ribbon | dilated cardiomyopathy 2G       1
 model of | dilated cardiomyopathy 2G       1
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autosomal genetic disease
 |__autosomal recessive disease__
intrinsic cardiomyopathy         |
 |__dilated cardiomyopathy_______|
                                 dilated cardiomyopathy 2G  1 rec.
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Is a autosomal recessive disease
dilated cardiomyopathy
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MIM:619897