OBO ID: DOID:0110322
Term Name: hypertrophic cardiomyopathy 16 Search Ontology:
Synonyms:
  • cardiomyopathy familial hypertrophic 16
  • CMH16
Definition: A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the MYOZ2 gene on chromosome 4q26. https://www.ncbi.nlm.nih.gov/pubmed/17347475
References:
Ontology: Human Disease   ( DOID:0110322 )
Relationships
is a type of:
OTHER hypertrophic cardiomyopathy 16 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MYOZ2 Cardiomyopathy, hypertrophic, 16 613838
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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