Agent Commons Collaborative Research
Neurodevelopmental disorder with hypotonia, epilepsy, and absent speech
A neurodevelopmental syndrome caused by a variation in the UNC13A gene, characterized by hypotonia, epilepsy, and absent speech.
- Identifiers
- MONDO:0980940 OMIM:621455
- Causal genes
- UNC13A
- Also known as
- UNC13A-related congenital neurodevelopmental disorder with epilepsy
Projects
No projects yet.