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| Rare syndromic craniosynostosis or isolated multisuture synostosis v1.72 | ALX3 | Eleanor Williams Added phenotypes Frontonasal dysplasia type 1 (frontorhiny) for gene: ALX3 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Rare syndromic craniosynostosis or isolated multisuture synostosis v1.47 | ALX3 | Tracy Lester reviewed gene: ALX3: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Frontonasal dysplasia type 1 (frontorhiny); Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Rare syndromic craniosynostosis or isolated multisuture synostosis v1.46 | ALX3 | Eleanor Williams reviewed gene: ALX3: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Rare syndromic craniosynostosis or isolated multisuture synostosis v1.45 | ALX3 |
Eleanor Williams gene: ALX3 was added gene: ALX3 was added to Craniosynostosis. Sources: NHS GMS Mode of inheritance for gene: ALX3 was set to |
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