DRS1Robinow syndrome, autosomal dominant 1WNT5A autosomal dominant Robinow syndromeautosomal dominant Robinow syndrome caused by mutation in WNT5Adysostosis acral with facial and genital abnormalitiesRobinow dwarfismacral dysostosis with Facial and genital abnormalitiesfetal face syndromefoetal face syndrome
Definition
Any autosomal dominant Robinow syndrome in which the cause of the disease is a mutation in the WNT5A gene.
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