Catalog
Chimaera 46, XX, 46, XY
Link to WHO Definition
Chimaera 46, XX, 46, XY – http://id.who.int/icd/entity/1262245334
A disease caused by XX and XY embryonic fusion or two distinct loss events of a sex chromosome from an XXY embryo early in development. This results in a subset of cells in the body having an XX karyotype, while other cells demonstrate an XY karyotype. This disease may present with abnormal genital development.