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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
dilated cardiomyopathy 3B  
A dilated cardiomyopathy that has_material_basis_in mutation in the gene encoding dystrophin (DMD) on chromosome Xp21. (DO)

Synonyms
Primary IDs: OMIM:302045
Definition Sources: https://pubmed.ncbi.nlm.nih.gov/3574369/ "DO" "DO"

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