WormBase Tree Display for DO_term: DOID:0110316

DOID:0110316 Name: hypertrophic cardiomyopathy 10
  Status: Valid
  Definition: A familial hypertrophic cardiomyopathy that has_material_basis_in mutation in the MYL2 gene.
  Synonym: Exact: CMH10
      cardiomyopathy, familial hypertrophic, 10
  Parent: Is_a: DOID:0080326
  DB_info: Database: OMIM disease 608758
  Attribute_of: Gene_by_orthology: WBGene00003369
      WBGene00003370