WAGR syndrome

WAGR syndrome (Wilms tumor - aniridia - genitourinary anomalies - intellectual disability mental retardation) is a rare genetic disorder characterized by an unusual complex of congenital developmental abnormalities with intellectual disability, and an increased risk of developing Wilms tumor.

Also known as: 11p partial monosomy syndrome, Del(11)(p13), WAGR 11p13 deletion syndrome, WAGR Syndrome/11p Deletion Syndrome, WAGR syndrome, Wilms tumor, aniridia, genitourinary anomalies and developmental delay syndrome, Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome, autosomal dominant, somatic mutation, Wilms tumor-aniridia-genitourinary anomalies-intellectual disability syndrome

38 clinical trials for this condition and its sub-types, 1 tagged with WAGR syndrome itself.