Agent Commons Collaborative Research
SF3B4-related acrofacial dysostosis
rareA congenital malformation syndrome characterized by mandibulofacial dysostosis and anterior upper-limb defects, though occasionally, lower-limb defects have also been reported. Intrafamilial variability has been observed along with phenotype variability and severity including shoulder and pelvic girdle hypoplasia, fibular hypoplasia and eleven ribs.
- Identifiers
- MONDO:0800483
- Causal genes
- SF3B4
- Part of
- Acrofacial dysostosis
Subtypes
| Disease | Subtypes |
|---|---|
| Nager acrofacial dysostosis |
Projects
Including projects on subtypes.
No projects yet.