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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
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0012704 - dilated cardiomyopathy 1X |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee