WormBase Tree Display for DO_term: DOID:0110309

DOID:0110309 Name: hypertrophic cardiomyopathy 3
  Status: Valid
  Definition: A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the alpha-tropomyosin gene (TPM1) on chromosome 15q22.
  Synonym: Exact: CMH3
      cardiomyopathy familial hypertrophic 3
  Parent: Is_a: DOID:0080326
  DB_info: Database: OMIM disease 115196
  Attribute_of: Gene_by_orthology: WBGene00002978