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Summary Literature (1)
MIM:180700 - ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1; DRS1

Xenbase Genes: wnt5a, dvl1, dvl3

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0019978 - Robinow syndrome
MONDO:0024455 - autosomal dominant Robinow syndrome 1

Disease Ontology (DO):
DOID:0060766 - autosomal dominant Robinow syndrome 1