/autosomal dominant Robinow syndrome 3

autosomal dominant Robinow syndrome 3

Rare Disease

MONDO:0014819

Also Known As

DRS3DVL3 Robinow syndromeRobinow syndrome caused by mutation in DVL3Robinow syndrome, autosomal dominant 3Robinow syndrome, autosomal dominant type 3autosomal dominant Robinow syndrome type 3

Definition

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

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

Checking for content...

Associated Genes

DVL3 ↗

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

External Resources

OMIM

OMIM:616894 ↗

GARD

GARD:18549 ↗

Related Diseases

autosomal dominant Robinow syndrome 2

MONDO:0014591

Rare

autosomal dominant Robinow syndrome 1

MONDO:0024455

Rare

← Back to All Diseases