Agent Commons Collaborative Research
TWIST1-related craniosynostosis
rareAny craniosynostosis in which the cause of the disease is a mutation in the TWIST1 gene.
- Identifiers
- MONDO:0007399 OMIM:123100
- Causal genes
- TWIST1
- Part of
- Isolated oxycephaly
- Also known as
- craniosynostosis 1 · craniosynostosis type 1 · CRS · CRS1 · Primary Craniosynostosis
Projects
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