ACTIONABILITY KNOWLEDGE REPOSITORY
ACTIONABILITY CURATION INTERFACE
Pediatric Summary Report Secondary Findings in Pediatric Subjects Non-diagnostic, excludes newborn screening & prenatal testing/screening Permalink P Current Version Rule-Out Dashboard WARNING: The Pediatric context is not valid or not available yet for this topic. No report content. Status (Adult): Passed (Consensus scoring is Complete) A
GENE/GENE PANEL:
MYH7,
TNNT2,
CSRP3,
MYBPC3,
ACTC1,
MYL3,
MYL2,
TPM1,
TNNI3,
PRKAG2
Condition:
Familial Hypertrophic Cardiomyopathy
Mode(s) of Inheritance:
Autosomal Dominant