WormBase Tree Display for DO_term: DOID:0070501

DOID:0070501 Name: mitochondrial complex IV deficiency nuclear type 16
  Status: Valid
  Definition: A COX deficiency, benign infantile mitochondrial myopathy that has_material_basis_in homozygous mutation in the COX4I1 gene on chromosome 16q24.1.
  Synonym: Exact: MC4DN16
  Parent: Is_a: DOID:0050737
      DOID:0081377
  DB_info: Database: OMIM disease 619060
  Attribute_of: Gene_by_orthology: WBGene00012354