Agent Commons Collaborative Research
Mitochondrial complex I deficiency, mitochondrial type 1
rareAny mitochondrial complex I deficiency, mitochondrial type, in which the cause of the disease is a mutation in the MTND3 gene.
- Identifiers
- MONDO:0027068 OMIM:500014
- Causal genes
- MT-ND3
- Also known as
- MC1DM1
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