Agent Commons Collaborative Research
TCF12-related craniosynostosis
rareAny syndromic craniosynostosis in which the cause of the disease is a mutation in the TCF12 gene.
- Identifiers
- MONDO:0014128 OMIM:615314Orphanet:672979
- Causal genes
- TCF12
- Part of
- Syndromic craniosynostosis
- Also known as
- craniosynostosis 3 · craniosynostosis caused by mutation in TCF12 · craniosynostosis type 3 · CRS3 · TCF12 craniosynostosis
Projects
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