PomBase home

Disease association ontology term - MONDO:0016333 - familial dilated cardiomyopathy

Term summary

ID
MONDO:0016333
Name
familial dilated cardiomyopathy
Ontology or CV name
Disease association
Definition
A a genetic form of heart disease that occurs when heart (cardiac) muscle becomes thin and weakened in at least one chamber of the heart, causing the open area of the chamber to become enlarged (dilated). As a result, the heart is unable to pump blood as efficiently as usual. To compensate, the heart attempts to increase the amount of blood being pumped through the heart, leading to further thinning and weakening of the cardiac muscle. Over time, this condition results in heart failure.

Parents

Annotation

Disease association

MONDO:0032592 - cardiomyopathy, dilated, 2c

References:

Genes:

MONDO:0030300 - cardiomyopathy, dilated, 2D

References:

Genes:

MONDO:0859358 - cardiomyopathy, dilated, 2H

References:

Genes:

MONDO:0957545 - cardiomyopathy, dilated, 2I

References:

Genes:

MONDO:0008409 - congenital myopathy 7A, myosin storage, autosomal dominant

References:

Genes:

MONDO:0012808 - dilated cardiomyopathy 1AA

References:

Genes:

MONDO:0013198 - dilated cardiomyopathy 1EE

References:

Genes:

MONDO:0013339 - dilated cardiomyopathy 1GG

References:

Genes:

MONDO:0014073 - dilated cardiomyopathy 1II

References:

Genes:

MONDO:0013261 - dilated cardiomyopathy 1R

References:

Genes:

MONDO:0013262 - dilated cardiomyopathy 1S

References:

Genes:

MONDO:0012556 - DK1-congenital disorder of glycosylation

References:

Genes:

MONDO:0013968 - PGM1-congenital disorder of glycosylation

References:

Genes: