mitochondrial complex V (ATP synthase) deficiency nuclear type 5
Disease
mitochondrial complex V (ATP synthase) deficiency nuclear type 5
- Definition
A mitochondrial complex V (ATP synthase) deficiency that has_material_basis_in homozygous mutation in the ATP5F1D gene on chromosome 19p13.3.
- Synonyms
- Cross References
- Parent Terms
- Child Terms
- None
- Sources of Associations
Associated Genes
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