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ENJackson-Weiss Syndrome (JWS)
Alias:
Jws
Craniosynostosis-Midfacial Hypoplasia-Foot Abnormalities Syndrome
Craniosynostosis, Midfacial Hypoplasia, and Foot Abnormalities
Craniosynostosis-Midfacial Hypoplasia-Foot Abnormalities
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Jackson-Weiss Syndrome, also known as jws, is related to saethre-chotzen syndrome and bone disease. An important gene associated with Jackson-Weiss Syndrome is FGFR2 (Fibroblast Growth Factor Receptor 2), and among its related pathways/superpathways are Apoptotic Pathways in Synovial Fibroblasts and ERK Signaling. Affiliated tissues include bone, and related phenotypes are hypertelorism and broad hallux phalanx
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MALACARDS
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