PomBase home

Disease association ontology term - MONDO:0005201 - restrictive cardiomyopathy

Term summary

ID
MONDO:0005201
Name
restrictive cardiomyopathy
Ontology or CV name
Disease association
Definition
A type of heart disorder referring to the inability of the ventricles to fill with blood because the myocardium (heart muscle) stiffens and looses its flexibility. Causes include replacement of the myocardium with scar tissue, abnormal cellular infiltration of the myocardium, or deposition of a substance (e.g., amyloid) in the myocardium.

Parents

Annotation

Disease association

MONDO:0005201 - restrictive cardiomyopathy

References:

Genes:

MONDO:0030330 - cardiomyopathy, familial restrictive, 6

References:

Genes:

MONDO:0017694 - glycogen storage disease due to acid maltase deficiency, infantile onset

References:

Genes:

MONDO:0018485 - glycogen storage disease due to acid maltase deficiency, late-onset

References:

Genes:

MONDO:0009290 - glycogen storage disease II

References:

Genes: