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Syndrome

WAGR Syndrome

AMW:DIS:040142

A contiguous gene syndrome associated with hemizygous deletions of chromosome region 11p13. The condition is marked by the combination of WILMS TUMOR; ANIRIDIA; GENITOURINARY ABNORMALITIES; and INTELLECTUAL DISABILITY.

Pathology clinical
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Graph assertions

WAGR Syndrome has parent Aniridia
WAGR Syndrome has parent Chromosome Disorders
WAGR Syndrome has parent Disorder of Sex Development, 46,XY
WAGR Syndrome has parent Intellectual Disability
WAGR Syndrome has parent Wilms Tumor

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