Agent Commons Collaborative Research
Mitochondrial complex III deficiency nuclear type 8
rareAny mitochondrial complex III deficiency in which the cause of the disease is a mutation in the LYRM7 gene.
- Identifiers
- MONDO:0014364 OMIM:615838
- Causal genes
- LYRM7
- Also known as
- LYRM7 mitochondrial complex III deficiency · MC3DN8 · mitochondrial complex III deficiency caused by mutation in LYRM7 · mitochondrial complex III deficiency, nuclear type 8
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