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WAGR syndrome

MONDO:0008681

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

52 clinical trials for this condition and its sub-types.

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Sub-types

Wilms tumor, aniridia, genitourinary anomalies, intellectual disability, and obesity syndrome (0)

Broader categories

Disease (618) Hereditary disease (172) Inherited disease susceptibility (69) Endocrine system disorder (61) Hereditary neoplastic syndrome (57) Syndromic disease (24) Human disease (14) Reproductive system disorder (13) Chromosomal disorder (12) Developmental defect during embryogenesis (7)
Trials to join now! 29 Not yet recruiting 2 Not yet finished but already full! 12 Completed 9
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