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dilated cardiomyopathy

MONDO:0005021

Also known as: dilated cardiomyopathy, familial dilated cardiomyopathy, idiopathic dilation cardiomyopathy

MONDO:
MONDO:0005021
Orphanet:
217604
Rare disease97 associated genes

Description

Cardiomyopathy which is characterized by dilation and contractile dysfunction of the left and right ventricles. It may be idiopathic, or it may result from a myocardial infarction, myocardial infection, or alcohol abuse. It is a cause of congestive heart failure.

Associated genes

+87 more genes — install the extension to see the full list inline on any page.

External references

Sources: MONDO (CC BY 4.0), Open Targets (CC0), Orphanet (CC BY 4.0).

Not for sole clinical decision-making. Always verify against primary sources.