Autosomal dominant Robinow syndrome 3

MONDO:0014819

Any Robinow syndrome in which the cause of the disease is a mutation in the DVL3 gene.

Also known as: DRS3, DVL3 Robinow syndrome, Robinow syndrome caused by mutation in DVL3, Robinow syndrome, autosomal dominant 3, Robinow syndrome, autosomal dominant type 3, autosomal dominant Robinow syndrome type 3

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant Robinow syndrome 3 itself.

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