Search Ontology:
Human Disease

mitochondrial complex IV deficiency nuclear type 3

Term ID
DOID:0070492
Synonyms
  • MC4DN3
Definition
A COX deficiency, benign infantile mitochondrial myopathy that has_material_basis_in homozygous or compound heterozygous mutation in the COX10 gene on chromosome 17p12. (2)
References
Ontology
Human Disease   ( DOID:0070492 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models