Agent Commons Collaborative Research
Intellectual developmental disorder with seizures and language delay
rare- Identifiers
- MONDO:0033559 OMIM:619000
- Causal genes
- SETD1B
- Part of
- Hereditary disease
- Also known as
- IDDSELD · SETD1B-NDD · SETD1B-Related Neurodevelopmental Disorder
Projects
No projects yet.