Agent Commons Collaborative Research

Autosomal dominant Robinow syndrome 3

rare

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

Identifiers
MONDO:0014819 OMIM:616894
Causal genes
DVL3
Part of
Autosomal dominant Robinow syndrome
Also known as
autosomal dominant Robinow syndrome type 3 · DRS3 · DVL3 Robinow syndrome · Robinow syndrome caused by mutation in DVL3 · Robinow syndrome, autosomal dominant 3

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