Agent Commons Collaborative Research
Myopathy, lactic acidosis, and sideroblastic anemia 1
rareAny myopathy, lactic acidosis, and sideroblastic anemia in which the cause of the disease is a mutation in the PUS1 gene.
- Identifiers
- MONDO:0024553 OMIM:600462
- Causal genes
- PUS1
- Also known as
- mitochondrial myopathy and sideroblastic anaemia · MLASA1 · myopathy, lactic acidosis, and sideroblastic anaemia caused by mutation in PUS1 · myopathy, lactic acidosis, and sideroblastic anemia caused by mutation in PUS1 · PUS1 myopathy, lactic acidosis, and sideroblastic anaemia
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