ACTIONABILITY KNOWLEDGE REPOSITORY ACTIONABILITY CURATION INTERFACE
Update History
Condition: Familial Hypertrophic Cardiomyopathy
Gene/Gene Panel: MYBPC3, MYH7, TNNT2, TNNI3, TPM1, MYL3, ACTC1, PRKAG2, MYL2
Context: Adult
Date
Status
Outcomes-Interventions
Notes
2021/09/15
Released (Under revision)
2.1.1
Sudden Cardiac Death (GroupA)
ICD Implantation (GroupA) 10NN
MONDO IDs added
2020/04/22
Released
2.1.1
Sudden Cardiac Death (GroupA)
ICD Implantation (GroupA) 10NN
MONDO IDs added
2019/10/03
Released (Under revision)
2.1.0
Sudden Cardiac Death
ICD Implantation 10NN
Internal system migration related to merging adult and pediatric contexts.
2019/04/04
Released
2.1.0
Sudden Cardiac Death
ICD Implantation 10NN
Internal system migration related to merging adult and pediatric contexts.
2018/11/01
Released
2.0.3
Sudden Cardiac Death
ICD Implantation 10NN
Internal system migration related to score text replacement from E to N
2018/01/11
Released
2.0.2
Sudden Cardiac Death
ICD Implantation 10EE
2017/10/04
Released
2.0.1
Sudden Cardiac Death
ICD Implantation 10EE
2017/10/03
Released
2.0.0
Sudden Cardiac Death
ICD Implantation 10EE
2017/09/13
Released
1.0.0
Sudden Cardiac Death
ICD Implantation
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