Disease

Robinow Syndrome

About the Disease
Robinow Syndrome, also known as acral dysostosis with facial and genital abnormalities, is related to robinow syndrome, autosomal dominant 1 and robinow syndrome, autosomal dominant 3. An important gene associated with Robinow Syndrome is ROR2 (Receptor Tyrosine Kinase Like Orphan Receptor 2), and among its related pathways/superpathways are Signal Transduction and Nanog in Mammalian ESC Pluripotency. Affiliated tissues include bone, kidney and heart, and related phenotypes are short stature and hypertelorism

Common Targets
DVL3 | CST4 | GPC4 | CDX4 | KRT18 | PIK3C2B | SPTLC1 | POTEE | TENM4 | NXN | TNIP2 | ROR2 | DVL1 | WNT5A | NCOA3

疾病靶点研报
Robinow Syndrome

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