Craniosynostosis 5, susceptibility to

MONDO:0014232

Any craniosynostosis in which the cause of the disease is a mutation in the ALX4 gene.

Also known as: ALX4 craniosynostosis, craniosynostosis 5, susceptibility to, craniosynostosis caused by mutation in ALX4, CRS5, susceptibility to craniosynostosis 5

0 clinical trials for this condition and its sub-types, 0 tagged with Craniosynostosis 5, susceptibility to itself.

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↑ Inherited disease susceptibility (1316)

Including sub-types (0) Tagged with Craniosynostosis 5, susceptibility to (0)

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