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DO Term : hypertrophic cardiomyopathy 10 [DOID:0110316] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A familial hypertrophic cardiomyopathy that has_material_basis_in mutation in the MYL2 gene.
  • synonyms:
  • 608758,
  • OMIM:608758,
  • CMH10,
  • cardiomyopathy, familial hypertrophic, 10
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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