Autosomal dominant Robinow syndrome 1

MONDO:0024455

Any autosomal dominant Robinow syndrome in which the cause of the disease is a mutation in the WNT5A gene.

Also known as: DRS1, Robinow syndrome, autosomal dominant 1, WNT5A autosomal dominant Robinow syndrome, autosomal dominant Robinow syndrome caused by mutation in WNT5A, dysostosis acral with facial and genital abnormalities, Robinow dwarfism, acral dysostosis with Facial and genital abnormalities, fetal face syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant Robinow syndrome 1 itself.

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