disease has feature Aniridia Intellectual disability WAGR syndrome https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/6744 https://github.com/monarch-initiative/mondo/issues/6753 https://rarediseases.info.nih.gov/diseases/5528/wagr-syndrome https://www.malacards.org/card/wilms_tumor_aniridia_genitourinary_anomalies_and_impaired_intellectual_development_syndrome Wilms tumor-aniridia-genitourinary anomalies-mental retardation 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-gonadoblastoma-mental retardation syndrome chromosome 11p deletion UMLS:C0206115 deletion 11p SCTID:715215007 chromosome 11P13 deletion syndrome chromosome 11p deletion syndrome chromosome 11p13 deletion syndrome MONDO:0008681 WAGR 11p13 deletion syndrome NORD:1833 Del(11)(p13) DOID:14515 WAGR Syndrome/11p Deletion Syndrome Wilms tumor, aniridia, genitourinary anomalies, and intellectual disability syndrome MEDGEN:64512 11p monosomy AGR triad MESH:D017624 NCIT:C3718 Wilms tumor, aniridia, genitourinary anomalies, intellectual disability syndrome WAGR syndrome icd11.foundation:1858307812 monosomy 11p13 11p deletion syndrome partial monosomy 11p WAGR 11p partial monosomy syndrome Orphanet:893 Wilms tumor, aniridia, genitourinary anomalies, mental retardation syndrome Wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome OMIM:194072 deletion 11p13 GARD:0005528 Wilms tumor-aniridia-gonadoblastoma-intellectual disability syndrome 11p deletion Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome, autosomal dominant, somatic mutation WAGR Complex Wilms tumor-aniridia-genitourinary anomalies-intellectual disability syndrome Wilms tumor, aniridia, genitourinary anomalies and developmental delay syndrome monosomy 11p DECIPHER:35 hereditary neoplastic syndrome partial deletion of the short arm of chromosome 11 46,XY disorder of sex development