Spondylo-ocular Syndrome

About the Disease
Spondyloocular Syndrome, also known as spondylo-ocular syndrome, is related to hepatic veno-occlusive disease and cardiac arrest. An important gene associated with Spondyloocular Syndrome is XYLT2 (Xylosyltransferase 2). Affiliated tissues include eye, bone and cortex, and related phenotypes are short neck and hypertelorism

Common Targets
KRT33A | SRGAP3 | AMOT | FAM149B1 | NLGN2 | MYO15A | SLFN14 | ASB16 | TAX1BP1 | PRR29 | FKBP10 | TET1 | XYLT2 | GPR179 | G2064 | ARHGAP23 | CAND2 | AIPL1 | STARD3

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