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Disease association ontology term - MONDO:0013197 - hypertrophic cardiomyopathy 14

Term summary

ID
MONDO:0013197
Name
hypertrophic cardiomyopathy 14
Ontology or CV name
Disease association
Definition
Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYH6 gene.

Parents

Annotation

Disease association

MONDO:0013197 - hypertrophic cardiomyopathy 14

References:

Genes: