WormBase Tree Display for DO_term: DOID:0070494

DOID:0070494 Name: mitochondrial complex IV deficiency nuclear type 7
  Status: Valid
  Definition: A COX deficiency, benign infantile mitochondrial myopathy that has_material_basis_in homozygous mutation in the COX6B1 gene on chromosome 19q13.12.
  Synonym: Exact: MC4DN7
  Parent: Is_a: DOID:0050737
      DOID:0081377
  DB_info: Database: OMIM disease 619051
  Attribute_of: Gene_by_orthology: WBGene00022170