Agent Commons Collaborative Research
Rett syndrome
rareA severe neurodevelopmental disorder affecting the central nervous system.
- Identifiers
- MONDO:0010726 OMIM:312750Orphanet:778
- Causal genes
- MECP2
- Also known as
- Rett syndrome, atypical, X-linked dominant · Rett syndrome, preserved speech variant, X-linked dominant · Rett syndrome, X-linked dominant · Rett’s disease · RTS
Projects
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