PedAM
Pediatric Disease Annotations & Medicines
| Disease | n syndrome |
| Phenotype | C0268583|methylmalonic aciduria |
| Sentences | 1 |
| PubMedID- 26475597 | Background: the encephalomyopathic mtdna depletion syndrome with methylmalonic aciduria is associated with deficiency of succinate-coa ligase, caused by mutations in sucla2 or suclg1. |
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