mitochondrial complex V (ATP synthase) deficiency, nuclear type 1 (Q18553463)
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mitochondrial metabolism disease that has material basis in mutation in the ATPAF2 gene on chromosome 17p11
- MC5DN1
- Mitochondrial complex V deficiency
- MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1
- Complex 5 mitochondrial respiratory chain deficiency
- MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1; MC5DN1
- Mitochondrial Complex 5 (Atp Synthase) Deficiency, Atpaf2 Type
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | mitochondrial complex V (ATP synthase) deficiency, nuclear type 1 |
mitochondrial metabolism disease that has material basis in mutation in the ATPAF2 gene on chromosome 17p11 |
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