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Disease association ontology term - MONDO:0016340 - familial restrictive cardiomyopathy

Term summary

ID
MONDO:0016340
Name
familial restrictive cardiomyopathy
Ontology or CV name
Disease association
Definition
An instance of restrictive cardiomyopathy that is caused by an inherited modification of the individual's genome.

Parents

Annotation

Disease association

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: