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Summary Literature (0)
OMIM:616331 - ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2


Xenbase Genes: dvl1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008389 - autosomal dominant Robinow syndrome
MONDO:0014591 - autosomal dominant Robinow syndrome 2
MONDO:0019978 - Robinow syndrome

Disease Ontology (DO):
DOID:0060765 - autosomal dominant Robinow syndrome 2