/autosomal dominant Robinow syndrome 2

autosomal dominant Robinow syndrome 2

Rare Disease

MONDO:0014591

Also Known As

DRS2DVL1 autosomal dominant Robinow syndromeRobinow syndrome, autosomal dominant type 2autosomal dominant Robinow syndrome caused by mutation in DVL1autosomal dominant Robinow syndrome type 2Robinow syndrome, autosomal dominant 2

Definition

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

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Associated Genes

DVL1 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:616331 ↗

GARD

GARD:18548 ↗

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