dilated cardiomyopathy 3B

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Summary

Literature (0)

DOID:0081164 - dilated cardiomyopathy 3B

Disease Ontology Definition:A dilated cardiomyopathy that has_material_basis_in mutation in the gene encoding dystrophin (DMD) on chromosome Xp21.

Synonyms:

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: dmd.2, dmd, dmd

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): dilated cardiomyopathy (is_a), X-linked monogenic disease (is_a)