Details of Disease | DrugMAP

General Information of Disease (ID: DISBA1TN)

Disease Name	Familial cardiomyopathy
Synonyms	hereditary cardiomyopathy
Definition	An instance of cardiomyopathy that is caused by an inherited modification of the individual's genome.
Disease Hierarchy	DISMT2VZ: Cardiogenetic disease DISUPZRG: Cardiomyopathy DISBA1TN: Familial cardiomyopathy
Disease Identifiers	MONDO ID MONDO_0005217 UMLS CUI C0264789 MedGen ID 538845 SNOMED CT ID 35728003

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	Strong	Genetic Variation	[1]
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This Disease Is Related to 1 DTP Molecule(s)

Gene Name	DTP ID	Evidence Level	Mode of Inheritance	REF
SLC39A8	DTLPQGT	Strong	Genetic Variation	[2]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
FHOD3	OT1WUBQX	Strong	Genetic Variation	[2]
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References

1	Coupling interval variability of premature ventricular contractions in patients with different underlying pathology: an insight into the arrhythmia mechanism.J Interv Card Electrophysiol. 2018 Jan;51(1):25-33. doi: 10.1007/s10840-017-0309-8. Epub 2018 Jan 5.
2	Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy.PLoS One. 2017 Mar 15;12(3):e0172995. doi: 10.1371/journal.pone.0172995. eCollection 2017.