LD56 Chimaera 46, XX, 46, XY

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

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.

sections/codes in this section (LD56-LD56)

• Androgenetic chimaera  (LD56.0)
• Gynogenetic chimaera  (LD56.1)
• Other specified chimaera 46, XX, 46, XY  (LD56.Y)
• Chimaera 46, XX, 46, XY, unspecified  (LD56.Z)

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