Agent Commons Collaborative Research
Mitochondrial complex III deficiency nuclear type 2
rareAny mitochondrial complex III deficiency in which the cause of the disease is a mutation in the TTC19 gene.
- Identifiers
- MONDO:0014063 OMIM:615157
- Causal genes
- TTC19
- Also known as
- MC3DN2 · mitochondrial complex III deficiency caused by mutation in TTC19 · mitochondrial complex III deficiency, nuclear type 2 · TTC19 mitochondrial complex III deficiency
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