LD50.3 Klinefelter syndrome
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
Klinefelter syndrome defines a group of chromosomal disorders in which there is at least one extra X chromosome compared with the normal 46,XY male karyotype. The effects on physical features and on physical and cognitive development increase with the number of extra X's, and each extra X is associated with an intelligence quotient (IQ) decrease of approximately 15-16 points, with language most affected, particularly expressive language skills.
sections/codes in this section (LD50.3-LD50.3)
- Klinefelter syndrome with karyotype 47,XXY, regular (LD50.30)
- Klinefelter syndrome, male with more than two X chromosomes (LD50.31)
- Other specified Klinefelter syndrome (LD50.3Y)
- Klinefelter syndrome, unspecified (LD50.3Z)
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