OBO ID: DOID:0110321
Term Name: hypertrophic cardiomyopathy 15 Search Ontology:
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 hypertrophic cardiomyopathy 15 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
VCL Cardiomyopathy, hypertrophic, 15 613255
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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