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Summary Literature (0)
MIM:616894 - ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3; DRS3

Xenbase Genes: dvl3

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008389 - autosomal dominant Robinow syndrome
MONDO:0014819 - autosomal dominant Robinow syndrome 3
MONDO:0019978 - Robinow syndrome