WormBase Tree Display for DO_term: DOID:0080359

DOID:0080359 Name: mitochondrial complex IV deficiency nuclear type 9
  Status: Valid
  Definition: A COX deficiency, infantile mitochondrial myopathy that has_material_basis_in homozygous mutation in the COA5 gene on chromosome 2q11.
  Synonym: Exact (2)
  Parent: Is_a (2)
  DB_info: Database: OMIM disease 616500
  Attribute_of: Gene_by_orthology: WBGene00012483