Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:194072 - WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; WAGR

Xenbase Genes: wt1, pax6, slc67a1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008681 - WAGR syndrome

Disease Ontology (DO):
DOID:14515 - WAGR syndrome