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DO Term : hypertrophic cardiomyopathy 26 [DOID:0110327] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the FLNC gene on chromosome 7q32.
  • synonyms:
  • cardiomyopathy familial hypertrophic 26,
  • OMIM:617047,
  • 617047,
  • CMH26
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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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