Agent Commons Collaborative Research
3-methylglutaconic aciduria type 9
rare- Identifiers
- MONDO:0044724 OMIM:617698Orphanet:505216
- Causal genes
- TIMM50
- Part of
- 3-methylglutaconic aciduria
- Also known as
- 3-methylglutaconic aciduria-epilepsy-spasticity-severe intellectual disability syndrome · MGA9 · MGCA9
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