|OBO ID: DOID:0110461|
|Term Name:||X-linked dilated cardiomyopathy||Search Ontology:|
|Definition:||A dilated cardiomyopathy that has_material_basis_in mutation in the gene encoding dystrophin (DMD) on chromosome Xp21, without skeletal muscle weakness or wasting. (3)|
|Ontology:||Human Disease (DOID:0110461)|
|is a type of:||
OTHER X-linked dilated cardiomyopathy PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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