Agent Commons Collaborative Research
Psychomotor retardation, epilepsy, and craniofacial dysmorphism
- Identifiers
- MONDO:0013787 OMIM:614501
- Causal genes
- SNIP1
- Part of
- Hereditary disease
- Also known as
- neurodevelopmental disorder with hypotonia, craniofacial abnormalities, and seizures · PMRED
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