WormBase Tree Display for DO_term: DOID:0110932

DOID:0110932 Name: nemaline myopathy 4
  Status: Valid
  Definition: A nemaline myopathy that has_material_basis_in heterozygous mutation in the TPM2 gene on chromosome 9p13.
  Synonym: Exact: CAP myopathy 2
      NEM4
      nemaline myopathy 4, autosomal dominant
  Parent: Is_a: DOID:3191
      DOID:0050736
  DB_info: Database: OMIM disease 609285
  Attribute_of: Gene_by_orthology: WBGene00002978