disease has feature Aniridia Intellectual disability syndrome caused by partial chromosomal deletion WAGR syndrome 11p deletion 11p deletion syndrome 11p monosomy 11p partial monosomy syndrome AGR triad DOID:14515 Del(11)(p13) GARD:0001732 GARD:0005528 ICD10:Q87.8 MESH:D017624 MONDO:0008681 NCIT:C3718 OMIM:194072 Orphanet:893 SCTID:715215007 UMLS:C0206115 UMLS:C2931803 WAGR WAGR Complex 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. Wilms tumor, aniridia, genitourinary anomalies and developmental delay syndrome Wilms tumor, aniridia, genitourinary anomalies, and intellectual disability syndrome Wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome Wilms tumor, aniridia, genitourinary anomalies, intellectual disability syndrome Wilms tumor, aniridia, genitourinary anomalies, mental retardation syndrome Wilms tumor-aniridia-genitourinary anomalies-intellectual disability syndrome Wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome Wilms tumor-aniridia-gonadoblastoma-intellectual disability syndrome Wilms tumor-aniridia-gonadoblastoma-mental retardation syndrome chromosome 11P13 deletion syndrome chromosome 11p deletion chromosome 11p deletion syndrome chromosome 11p13 deletion syndrome deletion 11p deletion 11p13 https://rarediseases.info.nih.gov/diseases/5528/wagr-syndrome monosomy 11p monosomy 11p13 partial monosomy 11p syndromic urogenital tract malformation polymalformative genetic syndrome with increased risk of developing cancer syndromic genetic obesity partial deletion of the short arm of chromosome 11 inherited renal cancer-predisposing syndrome syndromic renal or urinary tract malformation syndrome with 46,XY disorder of sex development syndromic aniridia rare disease with glaucoma as a major feature