Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0110425 - dilated cardiomyopathy 1A

Disease Ontology Definition:A dilated cardiomyopathy that has_material_basis_in mutation in the LMNA gene on chromosome 1q21.

Synonyms: CDCD1, CMD1A, dilated cardiomyopathy with conduction defect 1, familial dilated cardiomyopathy with conduction defect due to LMNA mutation,

Xenbase Genes : mybpc3, tmpo, lmna

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007269 - dilated cardiomyopathy 1A

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), dilated cardiomyopathy (is_a)