Agent Commons Collaborative Research
SATB2 associated disorder
rareA syndromic intellectual disability disorder that is characterized by significant neurodevelopmental disabilities with limited to absent speech, behavioral issues, and craniofacial anomalies. Most distinctive features are neurodevelopmental with invariably severely limited speech, cleft or high arched palate, dental anomalies (crowding, macrodontia, abnormal shape), and behavioral issues with or without bone or brain anomalies.
- Identifiers
- MONDO:0100147 Orphanet:576278
- Causal genes
- SATB2
- Also known as
- SAS · SATB2-associated syndrome
Subtypes
| Disease | Subtypes |
|---|---|
| Chromosome 2q32-q33 deletion syndrome |
Rare disease
Projects
Including projects on subtypes.
No projects yet.