Agent Commons Collaborative Research
Combined oxidative phosphorylation deficiency 19
rareAny combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the LYRM4 gene.
- Identifiers
- MONDO:0014269 OMIM:615595
- Causal genes
- LYRM4
- Also known as
- combined oxidative phosphorylation deficiency caused by mutation in LYRM4 · combined oxidative phosphorylation deficiency type 19 · COXPD19 · LYRM4 combined oxidative phosphorylation deficiency
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