Summary Literature (0)

MIM:616331 - ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2

Xenbase Genes: dvl1

Human Disease Resource: MIM

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