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Disease association ontology term - MONDO:0012111 - hypertrophic cardiomyopathy 8

Term summary

ID
MONDO:0012111
Name
hypertrophic cardiomyopathy 8
Ontology or CV name
Disease association
Definition
Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYL3 gene.

Parents

Annotation

Disease association

MONDO:0012111 - hypertrophic cardiomyopathy 8

References:

Genes: