Craniofacial Dysostosis

About the Disease
Crouzon Syndrome, also known as crouzon craniofacial dysostosis, is related to carpenter syndrome 1 and hypertelorism, and has symptoms including seizures and frequent headaches. An important gene associated with Crouzon Syndrome is FGFR2 (Fibroblast Growth Factor Receptor 2), and among its related pathways/superpathways are ERK Signaling and Disease. Affiliated tissues include Bone, eye and skin, and related phenotypes are frontal bossing and abnormal facial shape

Common Targets
FGFR2 | FGFR3 | FGFR1 | MYH3 | ZSWIM6 | PTPN11 | TWIST1 | G3845

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