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Autosomal dominant Robinow syndrome 2

MONDO:0014591

Any autosomal dominant Robinow syndrome in which the cause of the disease is a mutation in the DVL1 gene.

Also known as: DRS2, DVL1 autosomal dominant Robinow syndrome, Robinow syndrome, autosomal dominant type 2, autosomal dominant Robinow syndrome caused by mutation in DVL1, autosomal dominant Robinow syndrome type 2, Robinow syndrome, autosomal dominant 2

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant Robinow syndrome 2 itself.

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Including sub-types (0) Tagged with Autosomal dominant Robinow syndrome 2 (0)

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