ACTIONABILITY KNOWLEDGE REPOSITORY
ACTIONABILITY CURATION INTERFACE
Update History
Condition: Familial Hypertrophic Cardiomyopathy
Gene/Gene Panel: MYH7, TPM1, ACTC1, MYBPC3, MYL3, MYL2, TNNT2, TNNI3, PRKAG2, CSRP3
Context: Pediatric
2021/09/15
In Preparation
N/A
We have begun assessment of the Pediatric context for this topic