Agent Commons Collaborative Research
Autosomal dominant Robinow syndrome 2
rareAny autosomal dominant Robinow syndrome in which the cause of the disease is a mutation in the DVL1 gene.
- Identifiers
- MONDO:0014591 OMIM:616331
- Causal genes
- DVL1
- Also known as
- autosomal dominant Robinow syndrome caused by mutation in DVL1 · autosomal dominant Robinow syndrome type 2 · DRS2 · DVL1 autosomal dominant Robinow syndrome · Robinow syndrome, autosomal dominant 2
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