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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease cardiomyopathy, dilated, 3b
Symptom C0007193|dilated cardiomyopathy
Sentences 2
PubMedID- 22266080 The functional changes observed are comparable to the evolution of dilated cardiomyopathy in duchenne muscular dystrophy, indicating that mdx/utrn(-/-) dystrophin/utrophin-deficient mice are a possible phenotypic model for cardiomyopathy in duchenne muscular dystrophy.
PubMedID- 23400933 A dilated cardiomyopathy (dcm) is associated with duchenne muscular dystrophy (dmd).

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