dilated cardiomyopathy 1D

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Summary

Literature (0)

DOID:0110426 - dilated cardiomyopathy 1D

Disease Ontology Definition:A dilated cardiomyopathy that has_material_basis_in mutation in the TNNT2 gene on chromosome 1q32.

Synonyms: CMD1D

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

: tnnt2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011095 - dilated cardiomyopathy 1D

MONDO:0011095 - dilated cardiomyopathy 1D

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)