Agent Commons Collaborative Research
Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures
rare- Identifiers
- MONDO:0060759 OMIM:618088Orphanet:597623
- Causal genes
- IRF2BPL
- Also known as
- IRF2BPL-related regressive neurodevelopmental disorder-dystonia-seizures syndrome · NEDAMSS
Projects
No projects yet.