46,XY intersex condition Frasier syndrome http://purl.bioontology.org/ontology/MEDDRA/10080313 http://purl.bioontology.org/ontology/MESH/D052159 http://purl.bioontology.org/ontology/SNOMEDCT/445431000 http://purl.obolibrary.org/obo/DOID_0050438 http://purl.obolibrary.org/obo/NCIT_C122805 https://en.wikipedia.org/wiki/Frasier_syndrome https://www.wikidata.org/wiki/Q5493754 A syndrome characterized by chronic kidney failure and gonadal dysgenesis in phenotypic females with karyotype of 46,XY or female individual with a normal 46,XX karyotype. It is caused by donor splice-site mutations of Wilms tumor suppressor gene on chromosome 11. autosomal chromosomal syndrome Frasier syndrome http://purl.bioontology.org/ontology/MEDDRA/10080313 http://purl.bioontology.org/ontology/MESH/D052159 http://purl.bioontology.org/ontology/SNOMEDCT/445431000 http://purl.obolibrary.org/obo/DOID_0050438 http://purl.obolibrary.org/obo/NCIT_C122805 https://en.wikipedia.org/wiki/Frasier_syndrome https://www.wikidata.org/wiki/Q5493754 A syndrome characterized by chronic kidney failure and gonadal dysgenesis in phenotypic females with karyotype of 46,XY or female individual with a normal 46,XX karyotype. It is caused by donor splice-site mutations of Wilms tumor suppressor gene on chromosome 11.