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DO Term : hypertrophic cardiomyopathy 3 [DOID:0110309] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the alpha-tropomyosin gene (TPM1) on chromosome 15q22.
  • synonyms:
  • cardiomyopathy familial hypertrophic 3,
  • 115196,
  • CMH3,
  • OMIM:115196
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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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