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Q99.2 – Fragile X chromosome
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Q99.811 – Usher syndrome, type 1
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Q98.4 – Klinefelter syndrome, unspecified
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Q97.9 – Sex chromosome abnormality, female phenotype, unspecified
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Q98.0 – Klinefelter syndrome karyotype 47, XXY
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Q98.1 – Klinefelter syndrome, male with more than two X chromosomes
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Q98.3 – Other male with 46, XX karyotype
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Q96.9 – Turner's syndrome, unspecified
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Q97.0 – Karyotype 47, XXX
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Q97.1 – Female with more than three X chromosomes