PedAM
Pediatric Disease Annotations & Medicines
| Disease | lactic acidosis |
| Phenotype | C0162671|melas syndrome |
| Sentences | 1 |
| PubMedID- 21724600 | The m.3243a>g mutation was described as the major cause of the melas syndrome (mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes). |
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