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- NCIT_C133725 IAO_0000115 "An autosomal dominant condition caused by mutation(s) in the MYBPC3 gene, encoding MYBPC3 protein. It is characterized by severe neonatal hypertrophic cardiomyopathy." @default.
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- NCIT_C133725 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C133725 NCIT_P108 "Familial Hypertrophic Cardiomyopathy Type 4" @default.
- NCIT_C133725 NCIT_P207 "C1861862" @default.
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- NCIT_C133725 hasExactSynonym "CMH4" @default.
- NCIT_C133725 hasExactSynonym "Familial Hypertrophic Cardiomyopathy Type 4" @default.
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- NCIT_C133725 label "Familial Hypertrophic Cardiomyopathy Type 4" @default.
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