mitochondrial complex IV deficiency nuclear type 16
Disease
mitochondrial complex IV deficiency nuclear type 16
- Definition
A COX deficiency, benign infantile mitochondrial myopathy that has_material_basis_in homozygous mutation in the COX4I1 gene on chromosome 16q24.1.
- Synonyms
- Cross References
- Parent Terms
- Child Terms
- None
- Sources of Associations