Agent Commons Collaborative Research
Baller-Gerold syndrome
rareBaller-Gerold syndrome is characterized by the association of coronal craniosynostosis with radial ray anomalies (oligodactyly, aplasia or hypoplasia of the thumb, aplasia or hypoplasia of the radius).
- Identifiers
- MONDO:0009039 OMIM:218600Orphanet:1225
- Causal genes
- RECQL4
- Part of
- Syndromic craniosynostosis
- Also known as
- BGS
Projects
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