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| Rare syndromic craniosynostosis or isolated multisuture synostosis v1.72 | FGF3 | Eleanor Williams Added phenotypes congenital deafness with inner ear agenesis, microtia and microdontia for gene: FGF3 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Rare syndromic craniosynostosis or isolated multisuture synostosis v1.47 | FGF3 | Tracy Lester reviewed gene: FGF3: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: congenital deafness with inner ear agenesis, microtia and microdontia; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Rare syndromic craniosynostosis or isolated multisuture synostosis v1.46 | FGF3 | Eleanor Williams reviewed gene: FGF3: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Rare syndromic craniosynostosis or isolated multisuture synostosis v1.45 | FGF3 |
Eleanor Williams gene: FGF3 was added gene: FGF3 was added to Craniosynostosis. Sources: NHS GMS Mode of inheritance for gene: FGF3 was set to |
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