OBO ID: DOID:0081163 |
Term Name: | dilated cardiomyopathy 2G | Search Ontology: | |
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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. https://pubmed.ncbi.nlm.nih.gov/31517052/ | ||
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Ontology: | Human Disease ( DOID:0081163 ) |
OTHER dilated cardiomyopathy 2G PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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