nuclear type mitochondrial complex I deficiency 12
Disease
nuclear type mitochondrial complex I deficiency 12
- Definition
A nuclear type mitochondrial complex I deficiency that has_material_basis_in hemizygous mutation in the NDUFA1 gene on chromosome Xq24.
- Synonyms
- Cross References
- Parent Terms
- Child Terms
- None
- Sources of Associations
Associated Genes
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