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Metadata
ID	DOID:0110426
Name	dilated cardiomyopathy 1D
Definition	A dilated cardiomyopathy that has_material_basis_in mutation in the TNNT2 gene on chromosome 1q32. https://www.ncbi.nlm.nih.gov/pubmed/11106718
Xrefs	ICD10CM:I42.0 MIM:601494
Synonyms	CMD1D [EXACT]
Parent Relationships	is_a autosomal dominant disease is_a dilated cardiomyopathy
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance