Baller-Gerold syndrome
MeSH: C536788ORPHA: 1223
Overview
synostosis characterized by coronal craniosynostosis, short stature, and aplasia or hypoplasia of the radial bone
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C536788Orphanet Code
ORPHA:1223Baller-Gerold syndrome
| MeSH | C536788 |
| Orphanet | ORPHA:1223 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO