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Summary Literature (0)
DOID:0110444 - dilated cardiomyopathy 1X

Disease Ontology Definition:A dilated cardiomyopathy that has_material_basis_in mutation in the FKTN gene on chromosome 9q31.

Synonyms: CMD1X, dilated cardiomyopathy with mild or no proximal muscle weakness

Xenbase Genes : fktn

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012704 - dilated cardiomyopathy 1X


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

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