46,XY intersex condition WAGR syndrome http://purl.bioontology.org/ontology/MESH/D017624 http://purl.bioontology.org/ontology/SNOMEDCT/715215007 http://purl.obolibrary.org/obo/DOID_14515 https://en.wikipedia.org/wiki/WAGR_syndrome https://www.wikidata.org/wiki/Q1892153 11p partial monosomy syndrome A chromosomal deletion syndrome that is a nephroblastoma that results in a rare genetic syndrome in which affected children are predisposed to develop Wilms tumor, Aniridia (absence of the colored part of the eye, the iris), genitourinary anomalies, and intellectual disabilities. The condition results from a deletion on chromosome 11 resulting in the loss of several genes. As such, it is one of the best studied examples of a condition caused by loss of neighboring (contiguous) genes. WAGR syndromes Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation Syndrome Wilms Tumor-Aniridia-Genital Anomalies-Retardation Syndrome Wilms Tumor-Aniridia-Genitourinary Anomalies-MR Syndrome Wilms Tumor-Aniridia-Gonadoblastoma-Mental Retardation Syndrome Wilms tumor-Aniridia-Genitourinary Anomalies-Mental Retardation syndrome Wilms tumor-aniridia syndrome aniridia-Wilms tumor syndrome chromosome 11p13 deletion syndrome microdeletion syndrome