OBO ID: DOID:0110318
Term Name: hypertrophic cardiomyopathy 12 Search Ontology:
Synonyms:
  • cardiomyopathy familial hypertrophic 12
  • CMH12
Definition: A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the CSRP3 gene on chromosome 11p15. https://www.ncbi.nlm.nih.gov/pubmed/12642359
References:
Ontology: Human Disease   ( DOID:0110318 )
Relationships
is a type of:
OTHER hypertrophic cardiomyopathy 12 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CSRP3 Cardiomyopathy, hypertrophic, 12 612124
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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