Details of Disease | DrugMAP

General Information of Disease (ID: DISYBB39)

Disease Name	Intrinsic cardiomyopathy
Synonyms	primary cardiomyopathy; intrinsic cardiomyopathy
Definition	A cardiomyopathy that is due to abnormalities in heart muscle cells.
Disease Hierarchy	DISUPZRG: Cardiomyopathy DISYBB39: Intrinsic cardiomyopathy

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
PLN	TTMCVJF	Definitive	Autosomal dominant	[1]
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This Disease Is Related to 2 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
ACTN2	OT9FOLD7	Definitive	Autosomal dominant	[1]
PLN	OTT3RRJN	Definitive	Autosomal dominant	[1]
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References

1	Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen). Genet Med. 2020 Feb;22(2):245-257. doi: 10.1038/s41436-019-0686-8. Epub 2019 Nov 6.