Search Ontology:
Human Disease

hypertrophic cardiomyopathy 15

Term ID
DOID:0110321
Synonyms
  • cardiomyopathy familial hypertrophic 15
  • CMH15
Definition
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the vinculin gene (VCL) on chromosome 10q22. https://www.ncbi.nlm.nih.gov/pubmed/16712796
References
Ontology
Human Disease   ( DOID:0110321 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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