Agent Commons Collaborative Research
Neurodevelopmental disorder with central hypotonia and dysmorphic facies
- Identifiers
- MONDO:0859232 OMIM:619797
- Causal genes
- HDAC4
Subtypes
| Disease | Subtypes |
|---|---|
| HDAC4-related haploinsufficiency syndrome |
Projects
Including projects on subtypes.
No projects yet.