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MIM:615529 - CRANIOSYNOSTOSIS 5, SUSCEPTIBILITY TO; CRS5
Xenbase Genes: alx4
Human Disease Resource: OMIM
MONDO:0014232 - craniosynostosis 5, susceptibility to |
MONDO:0018112 - isolated scaphocephaly |
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MONDO:0014232 - craniosynostosis 5, susceptibility to |
MONDO:0018112 - isolated scaphocephaly |