OBO ID: DOID:0110309
Term Name: hypertrophic cardiomyopathy 3 Search Ontology:
Synonyms:
  • cardiomyopathy familial hypertrophic 3
  • CMH3
Definition: A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the alpha-tropomyosin gene (TPM1) on chromosome 15q22. https://www.ncbi.nlm.nih.gov/pubmed/8205619
References:
Ontology: Human Disease   ( DOID:0110309 )
Relationships
is a type of:
OTHER hypertrophic cardiomyopathy 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TPM1 Cardiomyopathy, hypertrophic, 3 115196
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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